# FDA Inspection 1099061 - Protek Medical Products Inc - August 08, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/3dadecd5-4170-4854-8775-0b084e85ec80
Source feed: FDA_Inspections

> FDA Inspection 1099061 for Protek Medical Products Inc on August 08, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099061 - 2019-08-08](https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/47f30340-0937-42ef-a00d-5db9c3f69cd0)
- [FDA Inspection 989313 - 2016-10-06](https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/dbe932c7-f233-4267-b033-638885e27ec4)
- [FDA Inspection 989313 - 2016-10-06](https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/8d842143-af83-48e3-b851-f52fef0d2ce8)
- [FDA Inspection 863555 - 2014-01-21](https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/cc53b35a-3b94-47eb-a804-446c9bde524f)
- [FDA Inspection 863555 - 2014-01-21](https://www.globalkeysolutions.net/records/fda_inspections/protek-medical-products-inc/591f7c6f-28dc-49d5-ac6b-c665cd24e55f)

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

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