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FDA Inspection 1308838 — Cerovene Inc.

Cerovene Inc. — FEI 3005890568

The FDA completed an inspection of Cerovene Inc. on March 23, 2026 in Valley Cottage, NY. 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 23, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valley Cottage, NY (United States)

Facility

Other inspections at this facility

  • 1215341 (NAI Tue Aug 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1074159 (NAI Mon Nov 05 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1001439 (VAI Wed Feb 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924812 (VAI Mon May 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 852062 (VAI Tue Oct 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources