# Prestige Medical – FDA Inspection, Oct 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/prestige-medical/77e016c2-cf69-423b-ba8e-6335b5868bc7
Source feed: FDA_Inspections

> FDA inspection 1107415 of Prestige Medical, October 24, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1107415
- Company Name: Prestige Medical
- Inspection Date: 2019-10-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1271421 - 2025-01-23
- [FDA Inspection 1197590 - 2023-01-13](https://www.keypedia.com/records/fda_inspections/prestige-medical/6dd55a79-acee-4a2e-87f9-40c911c9ada0)
- 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

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