FDA inspection

Georg Alber GmbH & Co. KG: FDA inspection ending Sep 19, 2013

FDA inspection 850601 · Voluntary Action Indicated (VAI) · Renquishausen

Key facts

Inspection ID 850601
Firm Georg Alber GmbH & Co. KG
FEI number 3002807056
Address Lindenstr. 13
City Renquishausen
Country Germany
Fiscal year 2013
Inspection end date Sep 19, 2013
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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

Browse all FDA inspections