FDA Inspection 800745 — Cerovene Inc.

Cerovene Inc. — FEI 3005890568

The FDA completed an inspection of Cerovene Inc. on September 20, 2012 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
September 20, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valley Cottage, NY (United States)