FDA Inspection 1221535 — ReproTech LLC

ReproTech LLC — FEI 3023813954

The FDA completed an inspection of ReproTech LLC on Oct 20, 2023 in Trumbull, CT. 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 20, 2023
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Trumbull, CT (United States)