FDA inspection

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen): FDA inspection ending Jul 26, 2016

FDA inspection 981825 · No Action Indicated (NAI) · Ravensburg

Key facts

Inspection ID 981825
Firm Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
FEI number 3005987757
Address Mooswiesen 2
City Ravensburg
Country Germany
Fiscal year 2016
Inspection end date Jul 26, 2016
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
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 10–99 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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