FDA Inspection 1089182 — Cytovance Biologics Inc.
The FDA completed an inspection of Cytovance Biologics Inc. on May 9, 2019 in Oklahoma City, OK. 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
- May 9, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Oklahoma City, OK (United States)