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FDA Inspection 666592 — Impax Laboratories, LLC.

Impax Laboratories, LLC. — FEI 3004182921

The FDA completed an inspection of Impax Laboratories, LLC. on April 22, 2010 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
April 22, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

Facility

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Recent compliance actions

FDA data resources