Section 310(b) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C. 337(b)) authorizes States to enforce certain sections of the act in their own names, but provides that States must notify FDA before doing so. Section 100.2(d) (21 CFR 100.2 (d)) sets forth the information that a State must provide to FDA in a letter of notification when it intends to take enforcement action under the act against a particular food located in the State.
The latest form for State Enforcement Notifications expires 2021-07-31 and can be found here.
Document Name |
---|
Supporting Statement A |
Approved without change |
Extension without change of a currently approved collection | 2018-06-28 | |
Approved without change |
Extension without change of a currently approved collection | 2015-06-08 | |
Approved without change |
Extension without change of a currently approved collection | 2012-03-19 | |
Approved without change |
Extension without change of a currently approved collection | 2008-11-18 | |
Approved without change |
Extension without change of a currently approved collection | 2005-09-15 | |
Approved without change |
Extension without change of a currently approved collection | 2002-09-03 | |
Approved without change |
Extension without change of a currently approved collection | 1999-08-23 | |
Approved without change |
Reinstatement with change of a previously approved collection | 1996-10-25 | |
Approved with change |
No material or nonsubstantive change to a currently approved collection | 1993-04-06 | |
Approved without change |
New collection (Request for a new OMB Control Number) | 1992-03-12 |