# Procedure Products, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/procedure-products-inc/7fd29bd7-1dee-4c43-8b80-d6678a4c6d81

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

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## Details

- Name: Procedure Products, Inc.
- FEI Number: 3020778
- City: Vancouver
- State: Washington
- Country Name: United States
- Address Line 1: 1801 W Fourth Plain Blvd
- Zip Code: 98660

## Related Documents

- [FDA Inspection 1056202 - Procedure Products, Inc. - 2018-06-07](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/84a2e75d-b373-4647-bd59-40b2509788b3) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2018
- [FDA Inspection 1056202 - Procedure Products, Inc. - 2018-06-07](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/dd7f3968-b095-457d-b141-f0ec319bf05e) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2018
- [FDA Inspection 908610 - Procedure Products, Inc. - 2015-01-05](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/d05d79eb-0c22-406e-8e59-fb5c95676736) — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2015
- [FDA Inspection 908610 - Procedure Products, Inc. - 2015-01-05](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/0d19a56d-a1d9-4694-b0a5-24ad581ea07a) — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2015
- [FDA Inspection 799630 - Procedure Products, Inc. - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/aeb1ab39-c1f0-4ad2-aad9-88a1b6e59e6d) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2012
- [FDA Inspection 799630 - Procedure Products, Inc. - 2012-08-30](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/714bfbce-41a9-4224-91cb-72f3333f4bd2) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2012
- [FDA Inspection 679641 - Procedure Products, Inc. - 2010-08-25](https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/991e2f2c-26a9-431e-bdeb-52f7086f3b29) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 25, 2010

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