FDA Inspection 1034655 — Kimera Labs Inc

Kimera Labs Inc — FEI 3011069063

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