# Morton Salt Inc, Grand Saline, TX – FDA Inspections

Source: https://www.keypedia.com/companies/morton-salt-inc/e1b2d8e8-ae09-4a7a-9f38-e4b1df62a587

> Inspection records and compliance data for Morton Salt Inc in Grand Saline, Texas. 7 FDA inspections on record (1 OAI), 1 Form 483, last inspected February 07, 2025.

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## Details

- Name: Morton Salt Inc
- FEI Number: 1610635
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: 801 State Highway 110
- City: Grand Saline
- State: Texas
- Zip Code: 75140
- Country Name: United States
- Address: 801 State Highway 110, Grand Saline, Texas 75140, United States
- Country: United States

## Related Documents

- [483 - Morton Salt Inc - Unknown Date](https://www.keypedia.com/records/483/morton-salt-inc/a0948819-3363-4eb3-b299-2f7a0aa9b743) — source: FDA, date: Invalid Date
- FDA Inspection 1261634 - Morton Salt Inc - 2025-02-07 — source: FDA, date: February 7, 2025
- [FDA Inspection 1261634 - Morton Salt Inc - 2025-02-07](https://www.keypedia.com/records/fda_inspections/morton-salt-inc/f0c1fb6b-34e5-4b9f-a0e0-620e121e08c4) — classification: Official Action Indicated (OAI), source: FDA, date: February 7, 2025
- FDA Inspection 1147281 - Morton Salt Inc - 2021-07-22 — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2021
- FDA Inspection 1048325 - Morton Salt Inc - 2018-04-10 — source: FDA, date: April 10, 2018
- FDA Inspection 982797 - Morton Salt Inc - 2016-08-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2016
- FDA Inspection 911114 - Morton Salt Inc - 2015-01-08 — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2015
- FDA Inspection 804058 - Morton Salt Inc - 2012-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2012
- FDA Inspection 804058 - Morton Salt Inc - 2012-10-15 — classification: No Action Indicated (NAI), source: FDA, date: October 15, 2012
- FDA Inspection 603511 - Morton Salt Inc - 2009-08-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2009

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