# FDA Inspection 1192319 - EMSI - December 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/emsi/d24e09d5-88dc-49f9-b698-ab47f7671c26
Source feed: FDA_Inspections

> FDA Inspection 1192319 for EMSI on December 08, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1192319
- Company Name: EMSI
- Inspection Date: 2022-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.keypedia.com/companies/emsi/e0ee00bc-1ff0-4c20-997f-2001d9280480

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