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FDA Inspection
•Exmoor Plastics Ltd.•June 25, 2009

Exmoor Plastics Ltd. – FDA Inspection, Jun 25, 2009

Record Details

This FDA Inspection record concerns Exmoor Plastics Ltd., with an inspection on June 25, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Exmoor Plastics Ltd.
Inspection Date
June 25, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · ffc6cc64-e376-4ae4-a144-84b18cc61ab0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
596745
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.180Legibility
  2. 21 CFR 820.184(e)ID label, labeling

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Exmoor Plastics Ltd.

5
DateClassificationOfficeProject area
December 5, 2019VAICenter for Devices and Radiological HealthCompliance: Devices
August 29, 2014VAICenter for Devices and Radiological HealthCompliance: Devices
August 4, 2011VAICenter for Devices and Radiological HealthCompliance: Devices
August 3, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
June 24, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Exmoor Plastics Ltd.
  • FDA Inspection 1113203 - 2019-12-05
  • FDA Inspection 897329 - 2014-08-29
  • FDA Inspection 741931 - 2011-08-04
  • FDA Inspection 743024 - 2011-08-03
  • FDA Inspection 596965 - 2009-06-24

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