FDA Inspection 888881 — Impax Laboratories, LLC.

Impax Laboratories, LLC. — FEI 3004182921

The FDA completed an inspection of Impax Laboratories, LLC. on July 31, 2014 in Hayward, 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
July 31, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)