# FDA Inspection 1043579 - Biorep Technologies, Inc. - February 05, 2018

Source: https://www.keypedia.com/records/fda_inspections/biorep-technologies-inc/b9aee27e-d7e0-4fd0-b850-e31279e129d7
Source feed: FDA_Inspections

> FDA Inspection 1043579 for Biorep Technologies, Inc. on February 05, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043579
- Company Name: Biorep Technologies, Inc.
- Inspection Date: 2018-02-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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