FDA inspection

Solupharm Pharmazeutische Erzeugnisse Gmbh: FDA inspection ending Sep 22, 2014

FDA inspection 897666 · Voluntary Action Indicated (VAI) · Melsungen

Key facts

Inspection ID 897666
Firm Solupharm Pharmazeutische Erzeugnisse Gmbh
FEI number 3008255368
Address Industriestr. 3
City Melsungen
Country Germany
Fiscal year 2014
Inspection end date Sep 22, 2014
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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