FDA inspection

Fidelio Healthcare Limburg GmbH: FDA inspection ending Jul 17, 2025

FDA inspection 1335558 · Voluntary Action Indicated (VAI) · Limburg

Key facts

Inspection ID 1335558
Firm Fidelio Healthcare Limburg GmbH
FEI number 1000449371
City Limburg
Country Germany
Fiscal year 2025
Inspection end date Jul 17, 2025
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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