# FDA Inspection 1102030 - Brevet, Inc. - August 08, 2019

Source: https://www.keypedia.com/records/fda_inspections/brevet-inc/0b90f29b-8e25-42c7-997e-92b7dec547e0
Source feed: FDA_Inspections

> FDA Inspection 1102030 for Brevet, Inc. on August 08, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1102030
- Company Name: Brevet, Inc.
- Inspection Date: 2019-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102030 - 2019-08-08](https://www.keypedia.com/records/fda_inspections/brevet-inc/c972518d-22e9-41dd-a854-75d1e5ac6785)
- [FDA Inspection 939863 - 2015-08-27](https://www.keypedia.com/records/fda_inspections/brevet-inc/3ad64246-ad52-4429-8ceb-793056685e8f)
- [FDA Inspection 939863 - 2015-08-27](https://www.keypedia.com/records/fda_inspections/brevet-inc/9991ecde-d550-4d78-bc5f-59dbd471b82b)
- [FDA Inspection 669781 - 2010-06-30](https://www.keypedia.com/records/fda_inspections/brevet-inc/59d2fdcc-7f9f-4dc6-9232-1e946d25c9d7)

Company: https://www.keypedia.com/companies/brevet-inc/6a6fdedc-f94e-48b7-b78a-088201dd14e8

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