# FDA Inspection 1217671 - MIE America, Inc. - September 14, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/mie-america-inc/6789114c-4707-4eed-875b-93c15b956b85
Source feed: FDA_Inspections

> FDA Inspection 1217671 for MIE America, Inc. on September 14, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1217671
- Company Name: MIE America, Inc.
- Inspection Date: 2023-09-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1217671 - 2023-09-14](https://www.globalkeysolutions.net/records/fda_inspections/mie-america-inc/78217c41-869c-4acd-be83-625a6c000a77)
- [FDA Inspection 1037046 - 2018-01-08](https://www.globalkeysolutions.net/records/fda_inspections/mie-america-inc/b9e3a42d-cefc-4247-ae5c-51f563624cad)
- [FDA Inspection 1037046 - 2018-01-08](https://www.globalkeysolutions.net/records/fda_inspections/mie-america-inc/5f94b41c-9ca2-4d76-b3a9-ef5a4a92b77d)

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

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