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FDA Inspection
•Western/Scott Fetzer Company•May 27, 2010

Western/Scott Fetzer Company – FDA Inspection, May 27, 2010

Record Details

This FDA Inspection record concerns Western/Scott Fetzer Company, with an inspection on May 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Western/Scott Fetzer Company
Inspection Date
May 27, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · c10a0df6-c75f-4494-920a-b71090f6c57d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
663119
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 803.50(a)(2)Individual Report of Malfunction
  2. 21 CFR 820.25(b)Training records
  3. 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Western/Scott Fetzer Company

4
DateClassificationOfficeProject area
August 29, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
August 8, 2018Not classifiedCincinnati District Office
August 12, 2016VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
September 2, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Western/Scott Fetzer Company
  • FDA Inspection 1064635 - 2018-08-29
  • FDA Inspection 1134007 - 2018-08-08
  • FDA Inspection 981670 - 2016-08-12
  • FDA Inspection 889918 - 2014-09-02

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