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FDA Inspection 1116753 — Hovione LLC

Hovione LLC — FEI 3006106736

The FDA completed an inspection of Hovione LLC on January 22, 2020 in East Windsor, 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
January 22, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
East Windsor, NJ (United States)

Facility

Other inspections at this facility

  • 1269771 (NAI Wed Jun 11 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 953507 (VAI Wed Dec 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 829292 (NAI Fri Apr 26 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 724233 (NAI Mon May 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources