# FDA Inspection 1084230 - BRIGHTWATER MEDICAL, INC. - March 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/brightwater-medical-inc/3359e481-21cf-4d46-b3da-9649eccab011
Source feed: FDA_Inspections

> FDA Inspection 1084230 for BRIGHTWATER MEDICAL, INC. on March 13, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084230
- Company Name: BRIGHTWATER MEDICAL, INC.
- Inspection Date: 2019-03-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1084230 - 2019-03-13](https://www.keypedia.com/records/fda_inspections/brightwater-medical-inc/3b1b9c30-0e6c-497e-9fed-b4c7b17598ee)

Company: https://www.keypedia.com/companies/brightwater-medical-inc/4ff32601-1fbd-4cf0-9230-eca4f08d7f2c

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