# Controltek, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/controltek-inc/e10ebf71-31f8-437f-8330-e24838fde527

> Inspection records and compliance data for Controltek, Inc. in Vancouver, Washington. Access full analysis and detailed observations.

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## Details

- Name: Controltek, Inc.
- FEI Number: 3001452666
- City: Vancouver
- State: Washington
- Country Name: United States
- Address Line 1: 3905 Ne 112th Ave
- Zip Code: 98682

## Related Documents

- [483 - Controltek, Inc. - 2019-12-20](https://www.keypedia.com/records/483/controltek-inc/1f34c150-6a84-41cd-bece-3900f17a8e7c) — source: FDA, date: December 20, 2019
- [FDA Inspection 1113619 - Controltek, Inc. - 2019-12-20](https://www.keypedia.com/records/fda_inspections/controltek-inc/12446f3d-02e8-4b4a-ab46-8b8a79986f05) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2019
- [FDA Inspection 1113619 - Controltek, Inc. - 2019-12-20](https://www.keypedia.com/records/fda_inspections/controltek-inc/15969409-8059-4c37-8f14-d029f574a398) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2019
- [FDA Inspection 903934 - Controltek, Inc. - 2014-11-24](https://www.keypedia.com/records/fda_inspections/controltek-inc/18ae6711-2cef-416e-ab77-abf06112b936) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 24, 2014
- [FDA Inspection 806860 - Controltek, Inc. - 2012-11-13](https://www.keypedia.com/records/fda_inspections/controltek-inc/333f2a70-ea0d-4a77-b15e-148a0aba5b3c) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2012
- [FDA Inspection 662205 - Controltek, Inc. - 2010-05-14](https://www.keypedia.com/records/fda_inspections/controltek-inc/41bdaf2d-abf1-4c4b-aada-6a837f2a2869) — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2010
- [FDA Inspection 662205 - Controltek, Inc. - 2010-05-14](https://www.keypedia.com/records/fda_inspections/controltek-inc/6b6b5b4b-7244-430d-be41-9512b9ca5860) — classification: No Action Indicated (NAI), source: FDA, date: May 14, 2010

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