# Prestige Ameritech – FDA Inspection, Aug 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/prestige-ameritech/b80b56b7-91b7-45e3-b248-254ab2cf5ce0
Source feed: FDA_Inspections

> FDA inspection 1063422 of Prestige Ameritech, August 20, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063422
- Company Name: Prestige Ameritech
- Inspection Date: 2018-08-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1227701 - 2024-01-11
- [FDA Inspection 1084042 - 2019-03-27](https://www.keypedia.com/records/fda_inspections/prestige-ameritech/f415cb7d-3868-41c0-963e-75a00094671d)
- FDA Inspection 903287 - 2014-11-13

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maricelys-mercado/de7e9ebc-8421-4fab-942e-6674fbdb4b1c)

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