FDA inspection

Miltenyi Biotec Gmbh: FDA inspection ending May 29, 2015

FDA inspection 930835 · Voluntary Action Indicated (VAI) · Bergisch Gladbach

Key facts

Inspection ID 930835
Firm Miltenyi Biotec Gmbh
FEI number 3004112148
Address Friedrich-ebert-str. 68
City Bergisch Gladbach
Country Germany
Fiscal year 2015
Inspection end date May 29, 2015
Classification Voluntary Action Indicated (VAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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