FDA Inspection 1268427 — Transcoject GmbH

Transcoject GmbH — FEI 3002655329

The FDA completed an inspection of Transcoject GmbH on Apr 2, 2025 in Neumunster. 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 2, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Neumunster (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.