FDA inspection

Bayer Weimar GmbH und Co. KG: FDA inspection ending Dec 4, 2009

FDA inspection 636510 · Voluntary Action Indicated (VAI) · Weimar

Key facts

Inspection ID 636510
Firm Bayer Weimar GmbH und Co. KG
FEI number 3002808091
Address Dobereinerstr. 20
City Weimar
Country Germany
Fiscal year 2010
Inspection end date Dec 4, 2009
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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

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