# Zirlotts Gulf Products, Coden, AL – FDA Inspections

Source: https://www.keypedia.com/companies/zirlotts-gulf-products/50cbf396-9c7b-4807-8fb0-22ef7c965be9

> Inspection records and compliance data for Zirlotts Gulf Products in Coden, Alabama. 9 FDA inspections on record (1 OAI), last inspected August 27, 2024.

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## Details

- Name: Zirlotts Gulf Products
- FEI Number: 3001237957
- Address Line 1: 14735 Commodore Ave
- City: Coden
- State: Alabama
- Zip Code: 36523
- Country Name: United States
- Address: 14735 Commodore Ave, Coden, Alabama 36523, United States
- Country: United States

## Related Documents

- FDA Inspection 1250472 - Zirlotts Gulf Products - 2024-08-27 — classification: No Action Indicated (NAI), source: FDA, date: August 27, 2024
- FDA Inspection 1118226 - Zirlotts Gulf Products - 2020-01-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 31, 2020
- FDA Inspection 1100423 - Zirlotts Gulf Products - 2019-07-24 — source: FDA, date: July 24, 2019
- FDA Inspection 1012374 - Zirlotts Gulf Products - 2017-07-26 — source: FDA, date: July 26, 2017
- [FDA Inspection 878812 - Zirlotts Gulf Products - 2014-05-16](https://www.keypedia.com/records/fda_inspections/zirlotts-gulf-products/385152c0-1436-47ab-9b9d-209d4743e198) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 16, 2014
- FDA Inspection 703554 - Zirlotts Gulf Products - 2010-12-02 — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2010
- FDA Inspection 671993 - Zirlotts Gulf Products - 2010-07-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2010
- [FDA Inspection 658353 - Zirlotts Gulf Products - 2010-04-15](https://www.keypedia.com/records/fda_inspections/zirlotts-gulf-products/7e92e2a8-2306-437e-a9da-d0509c980e5b) — classification: Official Action Indicated (OAI), source: FDA, date: April 15, 2010
- [FDA Inspection 612575 - Zirlotts Gulf Products - 2009-09-17](https://www.keypedia.com/records/fda_inspections/zirlotts-gulf-products/f0ae1c30-cf0f-4f84-a41c-2cd2f80e03fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2009

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