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FDA Inspection
•WOM World Of Medicine AG•June 23, 2017

WOM World Of Medicine AG – FDA Inspection, Jun 23, 2017

Record Details

This FDA Inspection record concerns WOM World Of Medicine AG, with an inspection on June 23, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
WOM World Of Medicine AG
Inspection Date
June 23, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Richard K. Vogel (FDA Associated Person)
View Company Profile

ID · 98d0823e-41b5-473c-8c23-59a24cb43d7c

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1017635
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
  2. 21 CFR 820.198(e)Records of complaint investigation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of WOM World Of Medicine AG

2
DateClassificationOfficeProject area
July 21, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
July 14, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for WOM World Of Medicine AG
  • FDA Inspection 1177250 - 2022-07-21
  • FDA Inspection 739056 - 2011-07-14

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