# Biotex Inc. – FDA Inspection, Aug 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/biotex-inc/8f7b61cd-b0d1-4cd7-8f69-ca2b6def2447
Source feed: FDA_Inspections

> FDA inspection 1063111 of Biotex Inc., August 23, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063111
- Company Name: Biotex Inc.
- Inspection Date: 2018-08-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 722995 - 2011-05-02](https://www.keypedia.com/records/fda_inspections/biotex-inc/ea686e8d-1ffc-4458-b7ee-8d81a24be5b2)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/biotex-inc/c08cd2b6-3f38-4d1d-b5c9-33be1783c385

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