FDA inspection

Bayer Weimar GmbH und Co. KG: FDA inspection ending Nov 5, 2015

FDA inspection 948310 · No Action Indicated (NAI) · Weimar

Key facts

Inspection ID 948310
Firm Bayer Weimar GmbH und Co. KG
FEI number 3002808091
Address Dobereinerstr. 20
City Weimar
Country Germany
Fiscal year 2016
Inspection end date Nov 5, 2015
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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