FDA Inspection 1198266 — Cosway Company, Inc.

Cosway Company, Inc. — FEI 3000205953

The FDA completed an inspection of Cosway Company, Inc. on February 24, 2023 in Carson, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 24, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carson, CA (United States)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls
434221 CFR 211.142(b)Storage under appropriate conditions