FDA inspection

5N Plus Lubeck GmbH: FDA inspection ending Nov 9, 2018

FDA inspection 1074936 · Voluntary Action Indicated (VAI) · Lubeck

Key facts

Inspection ID 1074936
Firm 5N Plus Lubeck GmbH
FEI number 3002807159
Address Kaninchenborn 24-28
City Lubeck
Country Germany
Fiscal year 2019
Inspection end date Nov 9, 2018
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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