FDA inspection

WEBER MEDICAL GMBH: FDA inspection ending Jan 17, 2013

FDA inspection 817804 · Official Action Indicated (OAI) · Lauenforde

Key facts

Inspection ID 817804
Firm WEBER MEDICAL GMBH
FEI number 3007165178
Address Sohnreystr. 4
City Lauenforde
Country Germany
Fiscal year 2013
Inspection end date Jan 17, 2013
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices
Warning letter 394666

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes 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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