# Protek Medical Products Inc – FDA Inspection, Aug 8, 2019

Source: https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/47f30340-0937-42ef-a00d-5db9c3f69cd0
Source feed: FDA_Inspections

> FDA inspection 1099061 of Protek Medical Products Inc, August 08, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099061
- Company Name: Protek Medical Products Inc
- Inspection Date: 2019-08-08
- 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: 3

## Related Documents

- FDA Inspection 989313 - 2016-10-06
- [FDA Inspection 863555 - 2014-01-21](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/cc53b35a-3b94-47eb-a804-446c9bde524f)
- FDA Inspection 598379 - 2009-07-21

## Related Officers

- [Investigator](https://www.keypedia.com/people/eric-c-fox/218af117-1551-476f-80ba-172e2cd6baee)

Company: https://www.keypedia.com/companies/protek-medical-products-inc/f5424d95-6e68-44ee-b658-d8a1b59b323f

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