FDA inspection

Serumwerk Bernburg AG: FDA inspection ending Jan 12, 2018

FDA inspection 1040866 · Voluntary Action Indicated (VAI) · Bernburg (Saale)

Key facts

Inspection ID 1040866
Firm Serumwerk Bernburg AG
FEI number 3003903447
Address Hallesche Landstr. 105b
City Bernburg (Saale)
Country Germany
Fiscal year 2018
Inspection end date Jan 12, 2018
Classification Voluntary Action Indicated (VAI)
Project area Monitoring of Marketed Animal Drugs, Feed, and Devices
Product type Veterinary

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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