# FDA Inspection 995537 - Biorep Technologies, Inc. - December 06, 2016

Source: https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/f6045aef-b95e-4dac-b96b-50567854f87a
Source feed: FDA_Inspections

> FDA Inspection 995537 for Biorep Technologies, Inc. on December 06, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 995537
- Company Name: Biorep Technologies, Inc.
- Inspection Date: 2016-12-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1239221 - 2024-04-26](https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/c7363b82-5b62-45c9-9dd9-b626a6651d44)
- [FDA Inspection 1043579 - 2018-02-05](https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/ccac6af4-fd45-48d6-8489-771d24c033ba)
- [FDA Inspection 1043579 - 2018-02-05](https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/b9aee27e-d7e0-4fd0-b850-e31279e129d7)
- [FDA Inspection 995537 - 2016-12-06](https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/b1e45185-56fa-42fc-a682-0a4eedd54497)
- [FDA Inspection 995537 - 2016-12-06](https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/3bd1ad41-1cbc-4dc6-beac-731a901b21a2)

Company: https://www.keypedia.com/companies/biorep-technologies-inc/2a7c1340-6e3a-4d7d-933f-feda95c8fe22

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