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FDA Inspection 771823 — Alcami Corporation

Alcami Corporation — FEI 2210008

The FDA completed an inspection of Alcami Corporation on March 15, 2012 in Edison, NJ. 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
March 15, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edison, NJ (United States)

Facility

Other inspections at this facility

  • 1115853 (NAI Wed Dec 18 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044788 (VAI Mon Mar 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018965 (NAI Fri May 05 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 989639 (VAI Tue Aug 23 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941628 (VAI Wed Aug 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources