FDA Inspection 1120923 — Camellix, LLC

Camellix, LLC — FEI 3010539352

The FDA completed an inspection of Camellix, LLC on March 13, 2020 in Augusta, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 13, 2020
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Augusta, GA (United States)

Citations

IDCFRDescription
1586121 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
1589721 CFR 111.83(a)Reserve sample - collect, hold
1592721 CFR 111.103Written procedures - quality control operations