# Danisco USA Inc. DBA IFF, Saint Joseph, MO – FDA Inspections

Source: https://www.keypedia.com/companies/danisco-usa-inc-dba-iff/d9009ecb-9c8b-4050-986e-6067107433a6

> Inspection records and compliance data for Danisco USA Inc. DBA IFF in Saint Joseph, Missouri. 8 FDA inspections on record, last inspected February 18, 2025.

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## Details

- Name: Danisco USA Inc. DBA IFF
- FEI Number: 1925399
- Address Line 1: 4509 S 50th St
- City: Saint Joseph
- State: Missouri
- Zip Code: 64507
- Country Name: United States
- Address: 4509 S 50th St, Saint Joseph, Missouri 64507, United States
- Country: United States

## Related Documents

- FDA Inspection 1266737 - Danisco USA Inc. DBA IFF - 2025-02-18 — source: FDA, date: February 18, 2025
- FDA Inspection 1266737 - Danisco USA Inc. DBA IFF - 2025-02-18 — source: FDA, date: February 18, 2025
- FDA Inspection 1266737 - Danisco USA Inc. DBA IFF - 2025-02-18 — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2025
- [FDA Inspection 1266737 - Danisco USA Inc. DBA IFF - 2025-02-18](https://www.keypedia.com/records/fda_inspections/danisco-usa-inc-dba-iff/fc0d0722-9235-455b-889a-601c4de3cbdc) — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2025
- FDA Inspection 1266737 - Danisco USA Inc. DBA IFF - 2025-02-18 — classification: No Action Indicated (NAI), source: FDA, date: February 18, 2025
- FDA Inspection 1168610 - Danisco USA Inc. DBA IFF - 2022-04-27 — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2022
- FDA Inspection 1168610 - Danisco USA Inc. DBA IFF - 2022-04-27 — classification: No Action Indicated (NAI), source: FDA, date: April 27, 2022
- FDA Inspection 1114730 - Danisco USA Inc. DBA IFF - 2019-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2019
- FDA Inspection 1030224 - Danisco USA Inc. DBA IFF - 2017-10-30 — source: FDA, date: October 30, 2017
- FDA Inspection 1029442 - Danisco USA Inc. DBA IFF - 2017-07-14 — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2017

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