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FDA Inspection 929678 — Impax Laboratories, LLC.

Impax Laboratories, LLC. — FEI 3004182921

The FDA completed an inspection of Impax Laboratories, LLC. on May 8, 2015 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 8, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

Facility

Other inspections at this facility

  • 1080691 (NAI Fri Jan 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1023293 (NAI Wed Aug 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 974379 (VAI Wed May 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 888881 (VAI Thu Jul 31 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 815250 (OAI Thu Feb 28 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources