# Prestige Medical – FDA Inspection, Jan 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/prestige-medical/6dd55a79-acee-4a2e-87f9-40c911c9ada0
Source feed: FDA_Inspections

> FDA inspection 1197590 of Prestige Medical, January 13, 2023. Classification: No Action Indicated (NAI). Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197590
- Company Name: Prestige Medical
- Inspection Date: 2023-01-13
- 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 1271421 - 2025-01-23
- [FDA Inspection 1107415 - 2019-10-24](https://www.keypedia.com/records/fda_inspections/prestige-medical/77e016c2-cf69-423b-ba8e-6335b5868bc7)
- FDA Inspection 974724 - 2016-06-08
- [FDA Inspection 846664 - 2013-08-28](https://www.keypedia.com/records/fda_inspections/prestige-medical/732cab75-63c9-4b93-8f50-49812b953c9c)
- FDA Inspection 651875 - 2010-03-10

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.keypedia.com/companies/prestige-medical/1e0afc98-ace1-46b8-8406-09dfcf2aa05e

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