FDA Inspection 1241582 — Curiteva Inc.
The FDA completed an inspection of Curiteva Inc. on May 22, 2024 in Tanner, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 22, 2024
- Fiscal Year
- 2024
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Tanner, AL (United States)