FDA inspection

AAP Implantate Ag: FDA inspection ending Nov 19, 2009

FDA inspection 631136 · Voluntary Action Indicated (VAI) · Berlin

Key facts

Inspection ID 631136
Firm AAP Implantate Ag
FEI number 3001406084
Address Lorenzweg 5
City Berlin
Country Germany
Fiscal year 2010
Inspection end date Nov 19, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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
  • 10–99 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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