# Professional Warehouse & Distribution, Inc., Saint Paul, MN – FDA Inspections

Source: https://www.keypedia.com/companies/professional-warehouse-distribution-inc/bfd83981-3fe5-4d6a-8c19-5b449fa12256

> Inspection records and compliance data for Professional Warehouse & Distribution, Inc. in Saint Paul, Minnesota. 6 FDA inspections on record (1 OAI), 1 Form 483, last inspected June 04, 2019.

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## Details

- Name: Professional Warehouse & Distribution, Inc.
- FEI Number: 3004264479
- Address Line 1: 2117 Charles Ave
- City: Saint Paul
- State: Minnesota
- Zip Code: 55114
- Country Name: United States
- Address: 2117 Charles Ave, Saint Paul, Minnesota 55114, United States
- Country: United States

## Related Documents

- FDA Inspection 1096483 - Professional Warehouse & Distribution, Inc. - 2019-06-04 — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2019
- FDA Inspection 1048888 - Professional Warehouse & Distribution, Inc. - 2018-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2018
- [FDA Inspection 1013529 - Professional Warehouse & Distribution, Inc. - 2017-06-08](https://www.keypedia.com/records/fda_inspections/professional-warehouse-distribution-inc/5e26d179-3a26-4ab4-be94-d3dd8d625680) — classification: Official Action Indicated (OAI), source: FDA, date: June 8, 2017
- [FDA Inspection 955254 - Professional Warehouse & Distribution, Inc. - 2015-10-22](https://www.keypedia.com/records/fda_inspections/professional-warehouse-distribution-inc/ca7f3e01-54f6-46a3-9d94-c24726dbf9b2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2015
- [FDA Inspection 914521 - Professional Warehouse & Distribution, Inc. - 2015-02-17](https://www.keypedia.com/records/fda_inspections/professional-warehouse-distribution-inc/3c873830-0639-4941-88ce-da975f4fb099) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 17, 2015
- FDA Inspection 803300 - Professional Warehouse & Distribution, Inc. - 2012-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2012

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