FDA inspection

Transcoject GmbH: FDA inspection ending Apr 2, 2025

FDA inspection 1268427 · No Action Indicated (NAI) · Neumunster

Key facts

Inspection ID 1268427
Firm Transcoject GmbH
FEI number 3002655329
Address Rugenstr. 8
City Neumunster
Country Germany
Fiscal year 2025
Inspection end date Apr 2, 2025
Classification No Action Indicated (NAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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