# Protek Medical Products Inc - Inspection Records

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

> Inspection records and compliance data for Protek Medical Products Inc in Coralville, Iowa. Access full analysis and detailed observations.

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## Details

- Name: Protek Medical Products Inc
- FEI Number: 3001701594
- City: Coralville
- State: Iowa
- Country Name: United States
- Address Line 1: 4125 Westcor Ct
- Zip Code: 52241

## Related Documents

- [483 - Protek Medical Products Inc - 2019-08-08](https://www.keypedia.com/records/483/protek-medical-products-inc/6046ede0-8116-41a2-a13f-10c2557eac67) — source: FDA, date: August 8, 2019
- [FDA Inspection 1099061 - Protek Medical Products Inc - 2019-08-08](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/3dadecd5-4170-4854-8775-0b084e85ec80) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2019
- [FDA Inspection 1099061 - Protek Medical Products Inc - 2019-08-08](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/47f30340-0937-42ef-a00d-5db9c3f69cd0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2019
- [FDA Inspection 989313 - Protek Medical Products Inc - 2016-10-06](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/dbe932c7-f233-4267-b033-638885e27ec4) — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2016
- [FDA Inspection 989313 - Protek Medical Products Inc - 2016-10-06](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/8d842143-af83-48e3-b851-f52fef0d2ce8) — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2016
- [FDA Inspection 863555 - Protek Medical Products Inc - 2014-01-21](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/cc53b35a-3b94-47eb-a804-446c9bde524f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2014
- [FDA Inspection 863555 - Protek Medical Products Inc - 2014-01-21](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/591f7c6f-28dc-49d5-ac6b-c665cd24e55f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2014
- [FDA Inspection 598379 - Protek Medical Products Inc - 2009-07-21](https://www.keypedia.com/records/fda_inspections/protek-medical-products-inc/1b2036ca-4e03-4d61-a3a2-131088558104) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2009

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## Related Officers

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