# Aurora Products, Inc., Orange, CT – FDA Inspections

Source: https://www.keypedia.com/companies/aurora-products-inc/532edf48-a7f2-4a54-8153-b3389227e61c

> Inspection records and compliance data for Aurora Products, Inc. in Orange, Connecticut. 7 FDA inspections on record, 1 Form 483, last inspected September 23, 2026.

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## Details

- Name: Aurora Products, Inc.
- FEI Number: 3002286594
- Address Line 1: 205 Edison Rd
- City: Orange
- State: Connecticut
- Zip Code: 06477
- Country Name: United States
- Address: 205 Edison Rd, Orange, Connecticut 06477, United States
- Country: United States

## Related Documents

- [FDA Inspection 1332854 - Aurora Products, Inc. - 2026-09-23](https://www.keypedia.com/records/fda_inspections/aurora-products-inc/d2deae3f-7880-4eab-b87a-ef281800a8bf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2026
- [FDA Inspection 1258102 - Aurora Products, Inc. - 2025-01-08](https://www.keypedia.com/records/fda_inspections/aurora-products-inc/728805cb-6a71-450d-a6c1-75335a304976) — source: FDA, date: January 8, 2025
- FDA Inspection 1041692 - Aurora Products, Inc. - 2018-02-09 — source: FDA, date: February 9, 2018
- FDA Inspection 987919 - Aurora Products, Inc. - 2016-10-20 — source: FDA, date: October 20, 2016
- FDA Inspection 923971 - Aurora Products, Inc. - 2015-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2015
- FDA Inspection 643172 - Aurora Products, Inc. - 2010-01-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 28, 2010
- FDA Inspection 563266 - Aurora Products, Inc. - 2009-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2009

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