# George J Howe Company, Inc., Grove City, PA – FDA Inspections

Source: https://www.keypedia.com/companies/george-j-howe-company-inc/04d3259d-ec07-4ce3-84de-6b4020f12d04

> Inspection records and compliance data for George J Howe Company, Inc. in Grove City, Pennsylvania. 13 FDA inspections on record, last inspected June 17, 2026.

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## Details

- Name: George J Howe Company, Inc.
- FEI Number: 1317926
- Address Line 1: 629 W Main St
- City: Grove City
- State: Pennsylvania
- Zip Code: 16127
- Country Name: United States
- Address: 629 W Main St, Grove City, Pennsylvania 16127, United States
- Country: United States

## Related Documents

- FDA Inspection 1290433 - George J Howe Company, Inc. - 2026-06-17 — source: FDA, date: June 17, 2026
- FDA Inspection 1241055 - George J Howe Company, Inc. - 2024-06-07 — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2024
- FDA Inspection 1241055 - George J Howe Company, Inc. - 2024-06-07 — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2024
- FDA Inspection 1122453 - George J Howe Company, Inc. - 2020-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2020
- FDA Inspection 1122453 - George J Howe Company, Inc. - 2020-01-30 — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2020
- FDA Inspection 1038420 - George J Howe Company, Inc. - 2018-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2018
- FDA Inspection 1005619 - George J Howe Company, Inc. - 2017-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2017
- FDA Inspection 1005619 - George J Howe Company, Inc. - 2017-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2017
- FDA Inspection 1005619 - George J Howe Company, Inc. - 2017-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2017
- FDA Inspection 861156 - George J Howe Company, Inc. - 2014-01-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 3, 2014

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