FDA inspection

ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH: FDA inspection ending Apr 11, 2013

FDA inspection 830498 · Official Action Indicated (OAI) · Grosspostwitz/O.L.

Key facts

Inspection ID 830498
Firm ONTEX HYGIENEARTIKEL DEUTSCHLAND GMBH
FEI number 3001019699
Address Fabrikstr. 30
City Grosspostwitz/O.L.
Country Germany
Fiscal year 2013
Inspection end date Apr 11, 2013
Classification Official Action Indicated (OAI)
Project area Postmarket Assurance: Devices
Product type Devices
Warning letter 398575

At a glance

  • 1–9 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

Browse all FDA inspections