# FDA Inspection 1084042 - Prestige Ameritech - March 27, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/prestige-ameritech/b3edafb9-914b-43cb-b4f2-9ce20a9f51a6
Source feed: FDA_Inspections

> FDA Inspection 1084042 for Prestige Ameritech on March 27, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1084042
- Company Name: Prestige Ameritech
- Inspection Date: 2019-03-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1084042 - 2019-03-27](https://www.globalkeysolutions.net/records/fda_inspections/prestige-ameritech/f415cb7d-3868-41c0-963e-75a00094671d)
- [FDA Inspection 1063422 - 2018-08-20](https://www.globalkeysolutions.net/records/fda_inspections/prestige-ameritech/b80b56b7-91b7-45e3-b248-254ab2cf5ce0)
- [FDA Inspection 903287 - 2014-11-13](https://www.globalkeysolutions.net/records/fda_inspections/prestige-ameritech/be2bf71b-fe13-4e3b-98c9-c8b75d298d52)
- [FDA Inspection 903287 - 2014-11-13](https://www.globalkeysolutions.net/records/fda_inspections/prestige-ameritech/0b483e7d-dd3d-4343-9cc3-96ca88ffb202)

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

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