FDA Inspection 987795 — ReproTech, LLC.

ReproTech, LLC. — FEI 3004586709

The FDA completed an inspection of ReproTech, LLC. on May 4, 2016 in Coconut Creek, 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
May 4, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Coconut Creek, FL (United States)