The
public
reporting
burden
mentioned
on
the
original
form
implies
that
this
is
a
public-use
form,
which
if
true
normally
would
require
an
OMB number & expiration date.
DEPARTMENT
OF
HEALTH
AND
HUMAN SERVICES
Food and Drug Administration
Form Approved: OMB No. xxxx-xxxx
Expiration Date: xx/xx/xxxx
(See Burden Statement below.)
Privacy
Act
Statement.
In
accordance
with
28
CFR
Section
16.41(d)
personal
data
sufficient
to
identify
the
individuals
submitting
requests
by
mail
under
the
Privacy
Act
of
1974,
5
U.S.C.
Section
552a,
is
required.
The
purpose
of
this
solicitation
is
to
ensure
that
the
records
of
individuals
who
are
the
subject
of
Food
and
Drug
Administration
systems
of
records
are
not
wrongfully
disclosed
by
the
Agency.
Requests
will
not
be
processed
if
this
information
is
not
furnished.
False
information
on
this
form
may
subject
the
requester
to
criminal
penalties
under
18
U.S.C.
Section
1001
and/or
5
U.S.C.
Section
552a(i)(3).
Full Name of Requestor 1
Entry fields on many FDA forms are typically below the text label.
Citizenship Status 2 |
Social Security Number 3
Designer note: This is a “layout design” |
Current Address |
Date of Birth proof. Entry fields will be added and the form will be made as a “508 compliant” and functional Adobe “LiveCycle” PDF |
Place of Birth file after FDA approves this layout design. |
I
declare
under
penalty
of
perjury
under
the
laws
of
the
United
States
of
America
that
the
foregoing
is
true
and
correct,
and
that
I
am
the
person
named
above,
and
I
understand
that
any
falsification
of
this
statement
is
punishable
under
the
provisions
of
18
U.S.C.
Section
1001
by
a
fine
of
not
more
than
$10,000
or
by
imprisonment
of
not
more
than
five
years
or
both,
and
that
requesting
or
obtaining
any
record(s)
under
false
pretenses
is
punishable
under
the
provisions
of
5
U.S.C.
552a(i)(3)
by
a
fine
of
not
more
than
$5,000.
Signature 4
Date
On
a
form,
it
is
often
the
case
that
footnotes
come
immediately
after
the
section
to
which
they
pertain.
It
is
also
best
to
not
stretch
several
lines
of
small
type
across
a
full
page,
due
to
readability
issues.
So
the
width
here
is
somewhat
less.
1
Name
of
individual
who is the subject of
the
record(s) sought.
2 Individual submitting a request under the Privacy Act of 1974 must be either “a citizen of the United States or an alien lawfully admitted for permanent residence,” pursuant to 5 U.S.C. Section 552a(a)(2). Requests will be processed as Freedom of Information Act requests pursuant to 5 U.S.C. Section 552, rather than Privacy Act requests, for individuals who are not United States citizens or aliens lawfully admitted for permanent residence.
3 Providing your social security number is voluntary. You are asked to provide your social security number only to facilitate the identification of records relating to you. Without your social security number, the Agency may be unable to locate any or all records pertaining to you.
4
Signature
of
individual
who is the subject of
the
record sought.
OPTIONAL: Authorization to Release Information to Another Person
This form is also to be completed by a requester who is authorizing information relating to himself or herself to be released to another person. Further, pursuant to 5 U.S.C. Section 552a(b), I authorize the U.S. Department of Justice to release any and all information relating to me to the person named below:
The
FDA
PRA
office
requires
the
PRA
section
below
to
be
placed
on
FDA
public-use
forms.
The
old
OMB
address
no
longer
is
placed
in
the
section.
The
section
is
for
the
benefit
of
form
users
and
pertains
to
the
FDA
PRA
office,
and
it
often
is
placed
at
the
end
of
the
form.
Name
of
Person
(Print
or type)
This
section
applies
only
to
requirements
of
the
Paperwork
Reduction
Act
of
1995.
*DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 0.5 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to the address below:
Department of Health and Human Services
Food and Drug Administration
Office of Operations
Paperwork Reduction Act (PRA) Staff
“An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number.”
The “0.5 hours” amount above is the same amount of time as the “0.50 hours” on the old original we were given (both figures equal 30 minutes). Mathematically speaking it is not necessary to carry the
FORM
FDA
3975
(5/16)
figure out to the hundredths instead of simply the tenths (one decimal position).
PSC Publishing Services (301) 443-6740 EF
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
File Title | FDA-3975.indd |
Author | PSC Publishing Services |
File Modified | 0000-00-00 |
File Created | 2021-01-22 |