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FDA Inspection
•Windsor Beach Technologies, Inc•August 8, 2018

Windsor Beach Technologies, Inc – FDA Inspection, Aug 8, 2018

Record Details

This FDA Inspection record concerns Windsor Beach Technologies, Inc, with an inspection on August 8, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Windsor Beach Technologies, Inc
Inspection Date
August 8, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Katelyn A. Staub-Zamperini (Issuing Officer)
View Company Profile

ID · dbef3f2f-23b9-4e47-a41f-b4325637389b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1063253
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Windsor Beach Technologies, Inc

2
DateClassificationOfficeProject area
September 30, 2025NAICenter for Devices and Radiological HealthCompliance: Devices
April 1, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Windsor Beach Technologies, Inc
  • FDA Inspection 1293562 - 2025-09-30
  • FDA Inspection 969938 - 2016-04-01

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