# Cargill Flavor Systems Puerto Rico Inc., Arecibo, PR – FDA Inspections

Source: https://www.keypedia.com/companies/cargill-flavor-systems-puerto-rico-inc/f53670de-de6d-4550-b7a8-68beb5d4a5ac

> Inspection records and compliance data for Cargill Flavor Systems Puerto Rico Inc. in Arecibo, Puerto Rico. 3 FDA inspections on record (1 OAI), last inspected January 05, 2012.

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## Details

- Name: Cargill Flavor Systems Puerto Rico Inc.
- FEI Number: 3004044998
- Address Line 1: Road 652, km 1.0, Bo. Higuillales
- City: Arecibo
- State: Puerto Rico
- Zip Code: 00612
- Country Name: United States
- Address: Road 652, km 1.0, Bo. Higuillales, Arecibo, Puerto Rico 00612, United States
- Country: United States

## Related Documents

- [FDA Inspection 761664 - Cargill Flavor Systems Puerto Rico Inc. - 2012-01-05](https://www.keypedia.com/records/fda_inspections/cargill-flavor-systems-puerto-rico-inc/6d9f1106-2ad4-4f97-bfd2-151de677ca1c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 5, 2012
- FDA Inspection 643162 - Cargill Flavor Systems Puerto Rico Inc. - 2010-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2010
- FDA Inspection 643162 - Cargill Flavor Systems Puerto Rico Inc. - 2010-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2010
- FDA Inspection 643162 - Cargill Flavor Systems Puerto Rico Inc. - 2010-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2010
- FDA Inspection 556087 - Cargill Flavor Systems Puerto Rico Inc. - 2009-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2009
- [FDA Inspection 556087 - Cargill Flavor Systems Puerto Rico Inc. - 2009-01-13](https://www.keypedia.com/records/fda_inspections/cargill-flavor-systems-puerto-rico-inc/6e6ba40a-9b81-4b94-a276-d598f6fa57e1) — classification: Official Action Indicated (OAI), source: FDA, date: January 13, 2009
- FDA Inspection 556087 - Cargill Flavor Systems Puerto Rico Inc. - 2009-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2009

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