ONE YEAR
APPROVAL IS GRANTED WITH THE UNDERSTANDING THAT FDA WILL REVISE
THESE REGULATIONS WITHIN ONE YEAR TO REDUCE BURDEN ON THE
PUBLIC.
Inventory as of this Action
Requested
Previously Approved
08/31/1988
08/31/1988
41,882
0
0
1,466,783
0
0
0
0
0
THE PURPOSE OF THE RADIATION CONTROL
FOR HEALTH AND SAFETY ACT IS TO PROTECT THE PUBLIC FROM UNNECESSARY
EXPOSURE TO RADIATION FROM ELECTRONIC PRODUCTS. TO CARRY OUT THIS
RESPONSIBILITY, FDA MUST COLLE CERTAIN INFORMATION FROM THE
MANUFACTURERS AND DEALERS/DISTRIBUTORS ABOUT THE ELECTRONIC
PRODUCTS THEY SELL AND INSTALL. THIS REQUEST CONTAINS SEVERAL TYPES
OF INFORMATION COLLECTIONS AND RECORDKEEPING REQUIREMENTS.
On behalf of this Federal agency, I certify that
the collection of information encompassed by this request complies
with 5 CFR 1320.9 and the related provisions of 5 CFR
1320.8(b)(3).
The following is a summary of the topics, regarding
the proposed collection of information, that the certification
covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a
benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control
number;
If you are unable to certify compliance with any of
these provisions, identify the item by leaving the box unchecked
and explain the reason in the Supporting Statement.