# Aga Enterprises Ltd, Kahului, HI – FDA Inspections

Source: https://www.keypedia.com/companies/aga-enterprises-ltd/2eb3031a-6549-419f-ba6a-42c9be0ecd1b

> Inspection records and compliance data for Aga Enterprises Ltd in Kahului, Hawaii. 7 FDA inspections on record, 2 Form 483s, last inspected April 18, 2025.

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## Details

- Name: Aga Enterprises Ltd
- FEI Number: 3000207215
- Address Line 1: 251 Lalo St Ste K1
- City: Kahului
- State: Hawaii
- Zip Code: 96732
- Country Name: United States
- Address: 251 Lalo St Ste K1, Kahului, Hawaii 96732, United States
- Country: United States

## Related Documents

- [FDA Inspection 1267217 - Aga Enterprises Ltd - 2025-04-18](https://www.keypedia.com/records/fda_inspections/aga-enterprises-ltd/a19e3e64-f970-47a7-9db7-4a718198161a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2025
- FDA Inspection 1166793 - Aga Enterprises Ltd - 2022-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2022
- [FDA Inspection 1003174 - Aga Enterprises Ltd - 2017-02-22](https://www.keypedia.com/records/fda_inspections/aga-enterprises-ltd/f4942ffa-9595-4452-9ae5-a57da469d36d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 22, 2017
- FDA Inspection 883584 - Aga Enterprises Ltd - 2014-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2014
- FDA Inspection 725729 - Aga Enterprises Ltd - 2011-05-17 — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2011
- FDA Inspection 725729 - Aga Enterprises Ltd - 2011-05-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2011
- FDA Inspection 662242 - Aga Enterprises Ltd - 2010-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2010
- FDA Inspection 662242 - Aga Enterprises Ltd - 2010-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2010
- FDA Inspection 592913 - Aga Enterprises Ltd - 2009-06-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2009

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