# FDA Inspection 872272 - Coagusense, Inc. - March 31, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/coagusense-inc/fc26169c-f106-4064-b320-65356f2d38c7/
Source feed: FDA_Inspections

> FDA Inspection 872272 for Coagusense, Inc. on March 31, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 872272
- Company Name: Coagusense, Inc.
- Inspection Date: 2014-03-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 872272 - 2014-03-31](https://www.globalkeysolutions.net/api/records/fda_inspections/coagusense-inc/5f818eb0-c112-4efe-a21f-f73f68f2c787/)

Company: https://www.globalkeysolutions.net/companies/coagusense-inc/09077523-e86e-41cc-86f1-76d17cf03f19

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