# US BioTek Laboratories, Inc. – FDA Inspection, Nov 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/us-biotek-laboratories-inc/8cecdd01-4819-4009-9c95-ca478cb17628
Source feed: FDA_Inspections

> FDA inspection 1071744 of US BioTek Laboratories, Inc., November 14, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1071744
- Company Name: US BioTek Laboratories, Inc.
- Inspection Date: 2018-11-14
- 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: 7

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/us-biotek-laboratories-inc/33da3b18-d1d3-4651-b87b-5ee9faa7f654

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