# FDA Inspection 939035 - Bridger Biomed, Inc. - August 21, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/bridger-biomed-inc/617e4758-9e85-4bd6-bf13-6d13b79baf08
Source feed: FDA_Inspections

> FDA Inspection 939035 for Bridger Biomed, Inc. on August 21, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939035
- Company Name: Bridger Biomed, Inc.
- Inspection Date: 2015-08-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 736368 - 2011-07-18](https://www.globalkeysolutions.net/records/fda_inspections/bridger-biomed-inc/f5ff876a-4241-4f1a-b18f-f5d226f5d26c)
- [FDA Inspection 736368 - 2011-07-18](https://www.globalkeysolutions.net/records/fda_inspections/bridger-biomed-inc/f66ef983-4490-40cd-ba56-89e0fbfb96e2)

Company: https://www.globalkeysolutions.net/companies/bridger-biomed-inc/db9bb891-ba96-497a-a5a1-789bf4d02cce

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