# McKeon Products, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/mckeon-products-inc/3dda1a57-ea67-4d29-bddd-cfb8aa3f5d48

> Inspection records and compliance data for McKeon Products, Inc. in Warren, Michigan. Access full analysis and detailed observations.

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## Details

- Name: McKeon Products, Inc.
- FEI Number: 1818945
- City: Warren
- State: Michigan
- Country Name: United States
- Address Line 1: 25460 Guenther
- Zip Code: 48091

## Related Documents

- [483 - McKeon Products, Inc. - 2025-05-07](https://www.keypedia.com/records/483/mckeon-products-inc/eb0c8ad9-fc30-47da-81c0-8614a5579542) — source: FDA, date: May 7, 2025
- [FDA Inspection 1269738 - McKeon Products, Inc. - 2025-05-07](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/436ef173-46b3-4345-bd27-67f85824d372) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2025
- [FDA Inspection 1269738 - McKeon Products, Inc. - 2025-05-07](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/7ac70013-eda4-423b-8161-59e0132e5bbc) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2025
- [FDA Inspection 1269738 - McKeon Products, Inc. - 2025-05-07](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/80682ce0-2999-48d7-8673-5bc8ba5435c3) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2025
- [FDA Inspection 1269738 - McKeon Products, Inc. - 2025-05-07](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/5f8d46ec-6d14-4fe6-abbb-5cfba0b31f7d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2025
- [FDA Inspection 1048234 - McKeon Products, Inc. - 2018-04-11](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/232e233d-9dd5-4d71-aea3-302b3390f359) — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2018
- [FDA Inspection 1048234 - McKeon Products, Inc. - 2018-04-11](https://www.keypedia.com/records/fda_inspections/mckeon-products-inc/d17a5c30-0b45-4742-b1e4-5a3cc381bdb4) — classification: No Action Indicated (NAI), source: FDA, date: April 11, 2018

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