FDA inspection

Fidelio Healthcare Limburg GmbH: FDA inspection ending Sep 21, 2011

FDA inspection 748702 · No Action Indicated (NAI) · Limburg

Key facts

Inspection ID 748702
Firm Fidelio Healthcare Limburg GmbH
FEI number 1000449371
Address Mundipharmastr. 2
City Limburg
Country Germany
Fiscal year 2011
Inspection end date Sep 21, 2011
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
  • No 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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