# MIE America, Inc. – FDA Inspection, Jan 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/mie-america-inc/b9e3a42d-cefc-4247-ae5c-51f563624cad
Source feed: FDA_Inspections

> FDA inspection 1037046 of MIE America, Inc., January 08, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037046
- Company Name: MIE America, Inc.
- Inspection Date: 2018-01-08
- 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: 4

## Related Documents

- [FDA Inspection 1217671 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/mie-america-inc/78217c41-869c-4acd-be83-625a6c000a77)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

Company: https://www.keypedia.com/companies/mie-america-inc/a1a7c905-2644-442b-8b33-caddfb71a6ac

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