FDA inspection

AAP Implantate Ag: FDA inspection ending Feb 12, 2015

FDA inspection 917531 · No Action Indicated (NAI) · Berlin

Key facts

Inspection ID 917531
Firm AAP Implantate Ag
FEI number 3001406084
Address Lorenzweg 5
City Berlin
Country Germany
Fiscal year 2015
Inspection end date Feb 12, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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