FDA Inspection 853399 — ReproTech, LTD.

ReproTech, LTD. — FEI 3009746947

The FDA completed an inspection of ReproTech, LTD. on Oct 30, 2013 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
Oct 30, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Garland, TX (United States)