FDA inspection

CUP Laboratorien Dr. Freitag GmbH: FDA inspection ending May 8, 2015

FDA inspection 927930 · Voluntary Action Indicated (VAI) · Radeberg

Key facts

Inspection ID 927930
Firm CUP Laboratorien Dr. Freitag GmbH
FEI number 3010163518
Address Carl-Eschebach-Str. 7
City Radeberg
Country Germany
Fiscal year 2015
Inspection end date May 8, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
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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