FDA Inspection 1051843 — telaGen, LLC
The FDA completed an inspection of telaGen, LLC on Apr 30, 2018 in Mobile, 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
- Apr 30, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Mobile, AL (United States)