# FDA Inspection 1119552 - Euromed, Inc. - March 03, 2020

Source: https://www.keypedia.com/records/fda_inspections/euromed-inc/8ea9f8f8-c094-48ff-a605-f9ce3083c3e3
Source feed: FDA_Inspections

> FDA Inspection 1119552 for Euromed, Inc. on March 03, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1119552
- Company Name: Euromed, Inc.
- Inspection Date: 2020-03-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 1172707 - 2022-06-10](https://www.keypedia.com/records/fda_inspections/euromed-inc/dd8f9e7b-72c6-4186-a45f-8311a4ec7163)

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

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