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FDA Inspection
•Olympus Winter & IBE Gmbh•December 4, 2014

Olympus Winter & IBE Gmbh – FDA Inspection, Dec 4, 2014

Record Details

This FDA Inspection record concerns Olympus Winter & IBE Gmbh, with an inspection on December 4, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Olympus Winter & IBE Gmbh
Inspection Date
December 4, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · dc21dd38-5d53-427f-aa86-6ad098e4c508

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
909453
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

1
  1. 21 CFR 820.86Acceptance status

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Olympus Winter & IBE Gmbh

5
DateClassificationOfficeProject area
November 21, 2025Not classifiedOffice of Inspections and InvestigationsCompliance: Medical Devices
September 1, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
April 12, 2018Not classifiedOffice of Inspections and Investigations
January 26, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
December 3, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Olympus Winter & IBE Gmbh
  • FDA Inspection 1292176 - 2025-11-21
  • FDA Inspection 1179969 - 2022-09-01
  • FDA Inspection 1078175 - 2018-04-12
  • FDA Inspection 1002852 - 2017-01-26
  • FDA Inspection 634581 - 2009-12-03

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