FDA Inspection 1056641 — telaGen, LLC

telaGen, LLC — FEI 3013545790

The FDA completed an inspection of telaGen, LLC on Apr 18, 2018 in Montgomery, AL. 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
Apr 18, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Montgomery, AL (United States)