FDA Inspection 1051167 — Reproductive Diagnostics Inc
The FDA completed an inspection of Reproductive Diagnostics Inc on May 3, 2018 in Columbus, OH. 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 3, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Columbus, OH (United States)