# FDA Inspection 1172707 - Euromed, Inc. - June 10, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/euromed-inc/dd8f9e7b-72c6-4186-a45f-8311a4ec7163
Source feed: FDA_Inspections

> FDA Inspection 1172707 for Euromed, Inc. on June 10, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1172707
- Company Name: Euromed, Inc.
- Inspection Date: 2022-06-10
- 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 1172707 - 2022-06-10](https://www.globalkeysolutions.net/records/fda_inspections/euromed-inc/d624789e-c289-40b5-ac79-88a5b5b12294)
- [FDA Inspection 1119552 - 2020-03-03](https://www.globalkeysolutions.net/records/fda_inspections/euromed-inc/8ea9f8f8-c094-48ff-a605-f9ce3083c3e3)

Company: https://www.globalkeysolutions.net/companies/euromed-inc/d99867cf-3611-4bb9-809b-080350b3e095

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