FDA Inspection 1215341 — Cerovene Inc.

Cerovene Inc. — FEI 3005890568

The FDA completed an inspection of Cerovene Inc. on August 1, 2023 in Valley Cottage, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 1, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valley Cottage, NY (United States)