# Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers, Aransas Pass, TX – FDA Inspections

Source: https://www.keypedia.com/companies/aransas-pass-seafood-packers-llc-dba-erickson-jensen-seafood-packers/951ce532-859f-4cd7-82ba-24d8d5557c19

> Inspection records and compliance data for Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers in Aransas Pass, Texas. 5 FDA inspections on record, last inspected August 01, 2022.

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## Details

- Name: Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers
- FEI Number: 1628159
- Address Line 1: 420 Bigelow St
- City: Aransas Pass
- State: Texas
- Zip Code: 78336
- Country Name: United States
- Address: 420 Bigelow St, Aransas Pass, Texas 78336, United States
- Country: United States

## Related Documents

- FDA Inspection 1177395 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2022-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2022
- FDA Inspection 1008787 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2017-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2017
- FDA Inspection 877636 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2014-03-24 — classification: No Action Indicated (NAI), source: FDA, date: March 24, 2014
- FDA Inspection 728364 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2011-05-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2011
- [FDA Inspection 728364 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2011-05-23](https://www.keypedia.com/records/fda_inspections/aransas-pass-seafood-packers-llc-dba-erickson-jensen-seafood-packers/f44b9fb9-5a55-4687-9357-7ce27846779a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2011
- FDA Inspection 700208 - Aransas Pass Seafood Packers, LLC dba Erickson & Jensen Seafood Packers - 2010-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2010

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