# The Hain Celestial Group, Inc. - Worldwide HQ, Hoboken, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/the-hain-celestial-group-inc-worldwide-hq/d2c2e454-c6cf-47e4-908d-7f4c2e877f5b

> Inspection records and compliance data for The Hain Celestial Group, Inc. - Worldwide HQ in Hoboken, New Jersey. 6 FDA inspections on record, last inspected June 20, 2025.

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## Details

- Name: The Hain Celestial Group, Inc. - Worldwide HQ
- FEI Number: 1000522004
- Address Line 1: 221 River St
- City: Hoboken
- State: New Jersey
- Zip Code: 07030
- Country Name: United States
- Address: 221 River St, Hoboken, New Jersey 07030, United States
- Country: United States

## Related Documents

- FDA Inspection 1262613 - The Hain Celestial Group, Inc. - Worldwide HQ - 2025-06-20 — source: FDA, date: June 20, 2025
- FDA Inspection 1262613 - The Hain Celestial Group, Inc. - Worldwide HQ - 2025-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- FDA Inspection 1262613 - The Hain Celestial Group, Inc. - Worldwide HQ - 2025-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- [FDA Inspection 1230595 - The Hain Celestial Group, Inc. - Worldwide HQ - 2024-04-09](https://www.keypedia.com/records/fda_inspections/the-hain-celestial-group-inc-worldwide-hq/907e3529-e172-4c14-84dc-5be036965e25) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 9, 2024
- FDA Inspection 1113172 - The Hain Celestial Group, Inc. - Worldwide HQ - 2019-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2019
- FDA Inspection 1022672 - The Hain Celestial Group, Inc. - Worldwide HQ - 2017-08-01 — classification: No Action Indicated (NAI), source: FDA, date: August 1, 2017
- FDA Inspection 1006002 - The Hain Celestial Group, Inc. - Worldwide HQ - 2017-03-20 — classification: No Action Indicated (NAI), source: FDA, date: March 20, 2017
- FDA Inspection 596507 - The Hain Celestial Group, Inc. - Worldwide HQ - 2009-07-02 — classification: No Action Indicated (NAI), source: FDA, date: July 2, 2009

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