FDA Inspection 1034655 — Kimera Labs Inc
The FDA completed an inspection of Kimera Labs Inc on Oct 24, 2017 in Miramar, FL. 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
- Oct 24, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Miramar, FL (United States)