# Mercer Milling Co., Inc., Liverpool, NY – FDA Inspections

Source: https://www.keypedia.com/companies/mercer-milling-co-inc/22081d6e-b5df-4e4b-874d-2dec3a20d631

> Inspection records and compliance data for Mercer Milling Co., Inc. in Liverpool, New York. 7 FDA inspections on record, 2 Form 483s, last inspected January 05, 2024.

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## Details

- Name: Mercer Milling Co., Inc.
- FEI Number: 3004050004
- Address Line 1: 4698 Crossroads Park Dr
- City: Liverpool
- State: New York
- Zip Code: 13088
- Country Name: United States
- Address: 4698 Crossroads Park Dr, Liverpool, New York 13088, United States
- Country: United States

## Related Documents

- [FDA Inspection 1226506 - Mercer Milling Co., Inc. - 2024-01-05](https://www.keypedia.com/records/fda_inspections/mercer-milling-co-inc/48bbd7bd-2052-4a8e-bc1d-bd9eb421420e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2024
- [FDA Inspection 1088899 - Mercer Milling Co., Inc. - 2019-05-07](https://www.keypedia.com/records/fda_inspections/mercer-milling-co-inc/af72f209-dd53-43d8-bf07-259a3ed2756b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2019
- [FDA Inspection 1051559 - Mercer Milling Co., Inc. - 2018-05-10](https://www.keypedia.com/records/fda_inspections/mercer-milling-co-inc/ccf0cf11-3486-4798-b0c7-56df967b27f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2018
- [FDA Inspection 871462 - Mercer Milling Co., Inc. - 2014-03-26](https://www.keypedia.com/records/fda_inspections/mercer-milling-co-inc/f02c4905-0d36-4089-9d65-090bade76a40) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2014
- FDA Inspection 765596 - Mercer Milling Co., Inc. - 2012-02-01 — classification: No Action Indicated (NAI), source: FDA, date: February 1, 2012
- FDA Inspection 649939 - Mercer Milling Co., Inc. - 2010-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2010
- FDA Inspection 609925 - Mercer Milling Co., Inc. - 2009-08-21 — classification: No Action Indicated (NAI), source: FDA, date: August 21, 2009

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