# Poseidon Group International Inc, Paramount, CA – FDA Inspections

Source: https://www.keypedia.com/companies/poseidon-group-international-inc/82b8d3f4-9a18-40c2-9f90-a2810e6406e1

> Inspection records and compliance data for Poseidon Group International Inc in Paramount, California. 6 FDA inspections on record, 1 Form 483, last inspected June 03, 2024.

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## Details

- Name: Poseidon Group International Inc
- FEI Number: 3002685971
- Address Line 1: 7100 Jackson St
- City: Paramount
- State: California
- Zip Code: 90723
- Country Name: United States
- Address: 7100 Jackson St, Paramount, California 90723, United States
- Country: United States

## Related Documents

- FDA Inspection 1240445 - Poseidon Group International Inc - 2024-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2024
- [FDA Inspection 1096819 - Poseidon Group International Inc - 2019-07-17](https://www.keypedia.com/records/fda_inspections/poseidon-group-international-inc/3cc4d992-5f24-49a8-833c-4cb98185a827) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2019
- [FDA Inspection 960011 - Poseidon Group International Inc - 2016-02-19](https://www.keypedia.com/records/fda_inspections/poseidon-group-international-inc/05d00aad-f913-4631-8d92-382bce572484) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2016
- FDA Inspection 719403 - Poseidon Group International Inc - 2011-04-14 — classification: No Action Indicated (NAI), source: FDA, date: April 14, 2011
- [FDA Inspection 712086 - Poseidon Group International Inc - 2011-03-04](https://www.keypedia.com/records/fda_inspections/poseidon-group-international-inc/db5cd65c-3d4f-455d-a5ee-ea20ff9244a2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2011
- [FDA Inspection 678431 - Poseidon Group International Inc - 2010-09-03](https://www.keypedia.com/records/fda_inspections/poseidon-group-international-inc/354fc097-9782-4a02-b82d-fbd12e424860) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 3, 2010

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