# Biorep Technologies, Inc. – FDA Inspection, Dec 6, 2016

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

> FDA inspection 995537 of Biorep Technologies, Inc., December 06, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995537
- Company Name: Biorep Technologies, Inc.
- Inspection Date: 2016-12-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 1239221 - 2024-04-26
- FDA Inspection 1043579 - 2018-02-05

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

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