FDA Inspection 665509 — Cosway Company, Inc.

Cosway Company, Inc. — FEI 3000205953

The FDA completed an inspection of Cosway Company, Inc. on May 27, 2010 in Carson, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 27, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carson, CA (United States)