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FDA Inspection
•Hampton Medical Devices, LLC•December 3, 2018

Hampton Medical Devices, LLC – FDA Inspection, Dec 3, 2018

Record Details

This FDA Inspection record concerns Hampton Medical Devices, LLC, with an inspection on December 3, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Hampton Medical Devices, LLC
Inspection Date
December 3, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Edward E. Lockwood (Issuing Officer)
View Company Profile

ID · d97e6744-1586-4dcd-833f-cbc007209e0c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1073567
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

Other FDA inspections of Hampton Medical Devices, LLC

3
DateClassificationOfficeProject area
November 8, 2021VAICenter for Devices and Radiological HealthCompliance: Devices
August 12, 2015NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 15, 2012VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Hampton Medical Devices, LLC
  • FDA Inspection 1157183 - 2021-11-08
  • FDA Inspection 946075 - 2015-08-12
  • FDA Inspection 772394 - 2012-03-15

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