FDA Inspection 1067222 — CCRM Minneapolis
The FDA completed an inspection of CCRM Minneapolis on August 31, 2018 in Edina, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 31, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Edina, MN (United States)