FDA Inspection 1074159 — Cerovene Inc.

Cerovene Inc. — FEI 3005890568

The FDA completed an inspection of Cerovene Inc. on November 5, 2018 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
November 5, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valley Cottage, NY (United States)