FDA inspection

Reapplix: FDA inspection ending May 11, 2023

FDA inspection 1207681 · No Action Indicated (NAI) · Birkerod

Key facts

Inspection ID 1207681
Firm Reapplix
FEI number 3014326253
Address Bregnerodvej 133a
City Birkerod
Country Denmark
Fiscal year 2023
Inspection end date May 11, 2023
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

Browse all FDA inspections