FDA Inspection 840678 — Cosway Company, Inc.

Cosway Company, Inc. — FEI 3000205953

The FDA completed an inspection of Cosway Company, Inc. on July 11, 2013 in Carson, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 11, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carson, CA (United States)

Citations

IDCFRDescription
261921 CFR 211.198(b)(2)Complaint Investigation/Follow-Up Findings