# Grimmway Enterprises, Inc., Lamont, CA – FDA Inspections

Source: https://www.keypedia.com/companies/grimmway-enterprises-inc/04b64d59-a4d9-416d-a3e9-b4afd3bf0b5c

> Inspection records and compliance data for Grimmway Enterprises, Inc. in Lamont, California. 6 FDA inspections on record, 1 Form 483, last inspected June 20, 2019.

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## Details

- Name: Grimmway Enterprises, Inc.
- FEI Number: 1000523108
- Address Line 1: 12000 Main St
- City: Lamont
- State: California
- Zip Code: 93241
- Country Name: United States
- Address: 12000 Main St, Lamont, California 93241, United States
- Country: United States

## Related Documents

- FDA Inspection 1093670 - Grimmway Enterprises, Inc. - 2019-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2019
- [FDA Inspection 1093670 - Grimmway Enterprises, Inc. - 2019-06-20](https://www.keypedia.com/records/fda_inspections/grimmway-enterprises-inc/956233cb-9445-4435-9401-7da72edcc42c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2019
- FDA Inspection 1000688 - Grimmway Enterprises, Inc. - 2017-02-13 — source: FDA, date: February 13, 2017
- FDA Inspection 870226 - Grimmway Enterprises, Inc. - 2014-03-24 — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2014
- FDA Inspection 870226 - Grimmway Enterprises, Inc. - 2014-03-24 — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2014
- FDA Inspection 861732 - Grimmway Enterprises, Inc. - 2013-12-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 23, 2013
- FDA Inspection 861732 - Grimmway Enterprises, Inc. - 2013-12-23 — classification: No Action Indicated (NAI), source: FDA, date: December 23, 2013
- FDA Inspection 851373 - Grimmway Enterprises, Inc. - 2013-10-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 8, 2013
- FDA Inspection 851373 - Grimmway Enterprises, Inc. - 2013-10-08 — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2013
- FDA Inspection 786193 - Grimmway Enterprises, Inc. - 2012-06-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 20, 2012

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