# Heller's Seafood Market, Inc., Warrington, PA – FDA Inspections

Source: https://www.keypedia.com/companies/hellers-seafood-market-inc/668ad7f4-9781-4575-98db-9b1a449a6d48

> Inspection records and compliance data for Heller's Seafood Market, Inc. in Warrington, Pennsylvania. 6 FDA inspections on record, 1 Form 483, last inspected November 22, 2019.

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## Details

- Name: Heller's Seafood Market, Inc.
- FEI Number: 3000719168
- Address Line 1: 1380 Easton Rd Ste 6
- City: Warrington
- State: Pennsylvania
- Zip Code: 18976
- Country Name: United States
- Address: 1380 Easton Rd Ste 6, Warrington, Pennsylvania 18976, United States
- Country: United States

## Related Documents

- FDA Inspection 1110740 - Heller's Seafood Market, Inc. - 2019-11-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 22, 2019
- FDA Inspection 1110740 - Heller's Seafood Market, Inc. - 2019-11-22 — classification: No Action Indicated (NAI), source: FDA, date: November 22, 2019
- [FDA Inspection 995765 - Heller's Seafood Market, Inc. - 2016-11-18](https://www.keypedia.com/records/fda_inspections/hellers-seafood-market-inc/0c7b4154-c2fc-4255-972c-ab74f5d92d29) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2016
- [FDA Inspection 890637 - Heller's Seafood Market, Inc. - 2014-08-07](https://www.keypedia.com/records/fda_inspections/hellers-seafood-market-inc/8f8c1bda-2885-48d2-912b-a0bd8017df4a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 7, 2014
- [FDA Inspection 715381 - Heller's Seafood Market, Inc. - 2011-03-23](https://www.keypedia.com/records/fda_inspections/hellers-seafood-market-inc/b70acb2a-5051-47f9-bcba-daa9b9a23e2a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2011
- FDA Inspection 667985 - Heller's Seafood Market, Inc. - 2010-06-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 10, 2010
- FDA Inspection 602269 - Heller's Seafood Market, Inc. - 2009-08-04 — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2009

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