# Magalhaes, Inc., New Bedford, MA – FDA Inspections

Source: https://www.keypedia.com/companies/magalhaes-inc/b01ad6c3-aeac-4576-81c6-77940edc9146

> Inspection records and compliance data for Magalhaes, Inc. in New Bedford, Massachusetts. 7 FDA inspections on record, 3 Form 483s, last inspected January 16, 2025.

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## Details

- Name: Magalhaes, Inc.
- FEI Number: 3004659126
- Address Line 1: 488 Belleville Ave
- City: New Bedford
- State: Massachusetts
- Zip Code: 02746
- Country Name: United States
- Address: 488 Belleville Ave, New Bedford, Massachusetts 02746, United States
- Country: United States

## Related Documents

- [FDA Inspection 1260671 - Magalhaes, Inc. - 2025-01-16](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/dc5ac829-319d-425a-a701-65e7242e8fc5) — source: FDA, date: January 16, 2025
- [FDA Inspection 1073709 - Magalhaes, Inc. - 2018-11-28](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/d51d7872-7a73-4866-88a3-3d3f61a9c7d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 28, 2018
- [FDA Inspection 1053066 - Magalhaes, Inc. - 2018-05-23](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/f4565631-5c17-4259-8dfe-d4c9dca24125) — source: FDA, date: May 23, 2018
- [FDA Inspection 887252 - Magalhaes, Inc. - 2014-07-10](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/101fcc11-6f8b-4d9c-ab5a-e002a2978f8c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 10, 2014
- [FDA Inspection 712900 - Magalhaes, Inc. - 2011-03-04](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/74a2bb9b-ec38-402b-b18f-f0f4328ddd44) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2011
- [FDA Inspection 640942 - Magalhaes, Inc. - 2010-01-26](https://www.keypedia.com/records/fda_inspections/magalhaes-inc/5b286f5b-bf87-49cc-a0a3-61f8b62a4acf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2010
- FDA Inspection 563279 - Magalhaes, Inc. - 2009-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2009

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