# Unilever Manufacturing (US), Inc., Sikeston, MO – FDA Inspections

Source: https://www.keypedia.com/companies/unilever-manufacturing-us-inc/bd8831ee-b39e-478e-b90e-9ce16d856a9d

> Inspection records and compliance data for Unilever Manufacturing (US), Inc. in Sikeston, Missouri. 8 FDA inspections on record, 3 Form 483s, last inspected July 14, 2025.

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## Details

- Name: Unilever Manufacturing (US), Inc.
- FEI Number: 3002915882
- Address Line 1: 2400 Rose Pkwy
- City: Sikeston
- State: Missouri
- Zip Code: 63801
- Country Name: United States
- Address: 2400 Rose Pkwy, Sikeston, Missouri 63801, United States
- Country: United States

## Related Documents

- [FDA Inspection 1263635 - Unilever Manufacturing (US), Inc. - 2025-07-14](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/fde2e7d7-b244-4b96-9a90-4fe4fb2aadc4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 14, 2025
- [FDA Inspection 1062822 - Unilever Manufacturing (US), Inc. - 2018-08-02](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/9dabd80a-531d-4ea1-a55a-be688af19713) — source: FDA, date: August 2, 2018
- [FDA Inspection 1007416 - Unilever Manufacturing (US), Inc. - 2017-03-23](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/6e689058-a571-49ec-9e75-fdbdf8d33bbc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2017
- [FDA Inspection 872776 - Unilever Manufacturing (US), Inc. - 2014-04-04](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/7b0cb8a1-0a5d-4ea7-bf61-58f73a435d0a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2014
- [FDA Inspection 873921 - Unilever Manufacturing (US), Inc. - 2014-04-04](https://www.keypedia.com/records/fda_inspections/unilever-manufacturing-us-inc/d0835a41-7bb5-4ae1-a5f5-794e3ac683f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2014
- FDA Inspection 739131 - Unilever Manufacturing (US), Inc. - 2011-08-04 — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2011
- FDA Inspection 673204 - Unilever Manufacturing (US), Inc. - 2010-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2010
- FDA Inspection 589375 - Unilever Manufacturing (US), Inc. - 2009-06-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 12, 2009

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