FDA Inspection 857668 — Axiom Laboratories

Axiom Laboratories — FEI 3011146631

The FDA completed an inspection of Axiom Laboratories on November 21, 2013 in Cedartown, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 21, 2013
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Cedartown, GA (United States)

Citations

IDCFRDescription
1554621 CFR 111.260(f)Batch record - yield
1556621 CFR 111.260(l)(3)Batch record - approved, released, rejected; batch
1581021 CFR 111.570(b)(2)Record - product complaint; good manufacturing practice
1588521 CFR 111.77(a)Specifications not met - reject, quality control