FDA inspection

Eurofins Dr. Specht International GmbH: FDA inspection ending Feb 2, 2018

FDA inspection 1039985 · Voluntary Action Indicated (VAI) · Hamburg

Key facts

Inspection ID 1039985
Firm Eurofins Dr. Specht International GmbH
FEI number 3005774220
Address Grosmoorbogen 25
City Hamburg
Country Germany
Fiscal year 2018
Inspection end date Feb 2, 2018
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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