FDA Warning Letter — Quality Supplement Manufacturing, Inc.

Case 637182 — FEI 3011606714

The FDA took a Warning Letter action against Quality Supplement Manufacturing, Inc. on December 13, 2022 (Oklahoma City, OK). The action was issued by CFSAN and concerns food/cosmetics products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Quality Supplement Manufacturing, Inc.
Date
December 13, 2022
Fiscal Year
2023
Product Type
Food/Cosmetics
Center
CFSAN
Location
Oklahoma City, OK (United States)