FDA Inspection 1046497 — Quality Supplement Manufacturing, Inc.

Quality Supplement Manufacturing, Inc. — FEI 3011606714

The FDA completed an inspection of Quality Supplement Manufacturing, Inc. on Mar 30, 2018 in Oklahoma City, OK. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 30, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Oklahoma City, OK (United States)

Citations

IDCFRDescription
1586621 CFR 111.75(a)(2)(ii)(E)Documentation - quality control, review, approve supplier
1590121 CFR 111.83(b)(3)Reserve sample - retained
1598621 CFR 111.123(b)(2)Quality control - batch, product specifications

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.