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

Source: https://www.keypedia.com/records/fda_inspections/windsor-beach-technologies-inc/dbef3f2f-23b9-4e47-a41f-b4325637389b
Source feed: FDA_Inspections

> FDA inspection 1063253 of Windsor Beach Technologies, Inc, August 08, 2018. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063253
- Company Name: Windsor Beach Technologies, Inc
- Inspection Date: 2018-08-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1293562 - 2025-09-30
- [FDA Inspection 969938 - 2016-04-01](https://www.keypedia.com/records/fda_inspections/windsor-beach-technologies-inc/a1082f4b-f9a5-4612-a439-f161b307afc7)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

Company: https://www.keypedia.com/companies/windsor-beach-technologies-inc/779bbf5d-6e6d-4d5f-9db6-22eb7db2a738

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7