FDA inspection

aap Biomaterials, GmbH: FDA inspection ending Sep 6, 2018

FDA inspection 1065580 · Official Action Indicated (OAI) · Dieburg

Key facts

Inspection ID 1065580
Firm aap Biomaterials, GmbH
FEI number 3005568854
Address Lagerstr. 11-15
City Dieburg
Country Germany
Fiscal year 2018
Inspection end date Sep 6, 2018
Classification Official Action Indicated (OAI)
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
  • 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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