# Unilever Supply Chain Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/unilever-supply-chain-inc/e4905b5b-1bcd-4f96-a1c1-f9ef122066f4

> Inspection records and compliance data for Unilever Supply Chain Inc in Owensboro, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Unilever Supply Chain Inc
- FEI Number: 1043373
- City: Owensboro
- State: Kentucky
- Country Name: United States
- Address Line 1: 1901 Ragu Dr
- Zip Code: 42303

## Related Documents

- [FDA Inspection 850056 - Unilever Supply Chain Inc - 2013-09-27](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/e07d750b-45ac-4ba7-abb0-8beba9ec28a2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2013
- [FDA Inspection 850056 - Unilever Supply Chain Inc - 2013-09-27](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/b9f1d235-69b1-43ab-ad37-03929803147c) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2013
- [FDA Inspection 845569 - Unilever Supply Chain Inc - 2013-08-15](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/97988cfd-0724-4848-9082-49080945fb8f) — classification: No Action Indicated (NAI), source: FDA, date: August 15, 2013
- [FDA Inspection 679052 - Unilever Supply Chain Inc - 2010-09-02](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/cd4c372e-f256-4cda-943e-124c3017d7a9) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2010
- [FDA Inspection 654035 - Unilever Supply Chain Inc - 2010-03-18](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/c6bcd5f8-4480-4c3f-ba92-fa53067293cb) — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2010
- [FDA Inspection 613734 - Unilever Supply Chain Inc - 2009-09-17](https://www.globalkeysolutions.net/records/fda_inspections/unilever-supply-chain-inc/3475f36c-ce68-4d03-8033-16932bb2593a) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2009

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