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FDA Inspection
•Oxford Performance Materials, Inc.•December 20, 2013

Oxford Performance Materials, Inc. – FDA Inspection, Dec 20, 2013

Record Details

This FDA Inspection record concerns Oxford Performance Materials, Inc., with an inspection on December 20, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company
Oxford Performance Materials, Inc.
Inspection Date
December 20, 2013
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fc3fb949-edc0-49f3-8418-751507f95725

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
861717
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 803.50(a)(1)Report of Death or Serious Injury

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Oxford Performance Materials, Inc.

4
DateClassificationOfficeProject area
October 8, 2026NAICenter for Devices and Radiological HealthCompliance: Devices
August 2, 2024VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
November 21, 2017VAICenter for Devices and Radiological HealthCompliance: Devices
April 7, 2017OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Oxford Performance Materials, Inc.
  • FDA Inspection 1341198 - 2026-10-08
  • FDA Inspection 1245812 - 2024-08-02
  • FDA Inspection 1034179 - 2017-11-21
  • FDA Inspection 1007636 - 2017-04-07

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