FDA inspection

Teva Biotech GmbH: FDA inspection ending Apr 26, 2013

FDA inspection 836491 · Voluntary Action Indicated (VAI) · Ulm

Key facts

Inspection ID 836491
Firm Teva Biotech GmbH
FEI number 3007817154
Address Dornierstr. 10
City Ulm
Fiscal year 2013
Inspection end date Apr 26, 2013
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
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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