# Cape Ann Seafood Exchange, Inc., Gloucester, MA – FDA Inspections

Source: https://www.keypedia.com/companies/cape-ann-seafood-exchange-inc/2e298f84-407f-4231-9bb0-7561c7150296

> Inspection records and compliance data for Cape Ann Seafood Exchange, Inc. in Gloucester, Massachusetts. 6 FDA inspections on record, 1 Form 483, last inspected January 08, 2018.

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## Details

- Name: Cape Ann Seafood Exchange, Inc.
- FEI Number: 3009113404
- Address Line 1: 27 Harbor Loop # 29
- City: Gloucester
- State: Massachusetts
- Zip Code: 01930
- Country Name: United States
- Address: 27 Harbor Loop # 29, Gloucester, Massachusetts 01930, United States
- Country: United States

## Related Documents

- [FDA Inspection 1037133 - Cape Ann Seafood Exchange, Inc. - 2018-01-08](https://www.keypedia.com/records/fda_inspections/cape-ann-seafood-exchange-inc/140a0eb1-2a48-4bb5-b426-06c81889d209) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 8, 2018
- [FDA Inspection 981427 - Cape Ann Seafood Exchange, Inc. - 2016-07-12](https://www.keypedia.com/records/fda_inspections/cape-ann-seafood-exchange-inc/74399ce6-5581-4c15-9e50-29e3a49f7fcf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 12, 2016
- FDA Inspection 860889 - Cape Ann Seafood Exchange, Inc. - 2013-12-17 — classification: No Action Indicated (NAI), source: FDA, date: December 17, 2013
- FDA Inspection 838100 - Cape Ann Seafood Exchange, Inc. - 2013-06-26 — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2013
- [FDA Inspection 697556 - Cape Ann Seafood Exchange, Inc. - 2010-11-10](https://www.keypedia.com/records/fda_inspections/cape-ann-seafood-exchange-inc/d3b9c369-0bee-4718-9eb5-fe014c6b592c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2010
- [FDA Inspection 612365 - Cape Ann Seafood Exchange, Inc. - 2009-09-09](https://www.keypedia.com/records/fda_inspections/cape-ann-seafood-exchange-inc/fdd4465c-e0d8-4053-b5cf-371ba483d9c7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 9, 2009

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