FDA Inspection 1007051 — ReproTech, LTD.
The FDA completed an inspection of ReproTech, LTD. on Mar 7, 2017 in Garland, TX. 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
- Mar 7, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Garland, TX (United States)