FDA Inspection 1102997 — Mayway Corporation

Mayway Corporation — FEI 3000209639

The FDA completed an inspection of Mayway Corporation on September 26, 2019 in Oakland, CA. 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
September 26, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Oakland, CA (United States)

Citations

IDCFRDescription
1552621 CFR 111.30(c)Equipment - automated - calibrate, inspect
1583921 CFR 111.70(e)Specifications - identity, purity, strength, composition
1593021 CFR 111.105Quality control - ensure quality; package, labeled, master record