FDA Inspection 974379 — Impax Laboratories, LLC.
The FDA completed an inspection of Impax Laboratories, LLC. on May 4, 2016 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
- May 4, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Hayward, CA (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)