# Prestige Ameritech – FDA Inspection, Mar 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/prestige-ameritech/f415cb7d-3868-41c0-963e-75a00094671d
Source feed: FDA_Inspections

> FDA inspection 1084042 of Prestige Ameritech, March 27, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084042
- Company Name: Prestige Ameritech
- Inspection Date: 2019-03-27
- 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: 2

## Related Documents

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- [FDA Inspection 1063422 - 2018-08-20](https://www.keypedia.com/records/fda_inspections/prestige-ameritech/b80b56b7-91b7-45e3-b248-254ab2cf5ce0)
- FDA Inspection 903287 - 2014-11-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/prestige-ameritech/0f0334bc-35d8-4eb8-b7a8-b994b7c55727

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