# Tropicana Products, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/tropicana-products-inc/9a37ae2d-17a0-42a5-8091-0c75f709608f

> Inspection records and compliance data for Tropicana Products, Inc. in Fort Pierce, Florida. Access full analysis and detailed observations.

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## Details

- Name: Tropicana Products, Inc.
- FEI Number: 1041685
- City: Fort Pierce
- State: Florida
- Country Name: United States
- Address Line 1: 6500 Glades Cut Off Rd
- Zip Code: 34981

## Related Documents

- [FDA Inspection 1285936 - Tropicana Products, Inc. - 2026-05-01](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/966b4171-f3de-4d61-a099-373d1b7fddd5) — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2026
- [FDA Inspection 1103487 - Tropicana Products, Inc. - 2019-09-09](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/eb2ea4d3-be36-47ec-9cb0-1c7f29612f86) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2019
- [FDA Inspection 979832 - Tropicana Products, Inc. - 2016-06-30](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/b3ec6c4b-8ca9-41fa-b726-31a8c1a85145) — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2016
- [FDA Inspection 817160 - Tropicana Products, Inc. - 2013-02-06](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/036815cc-f9e0-4d86-b428-079b10eb882f) — classification: No Action Indicated (NAI), source: FDA, date: February 6, 2013
- [FDA Inspection 590909 - Tropicana Products, Inc. - 2009-06-22](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/f72a9e85-d182-4791-9130-25bbf5b60640) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2009
- [FDA Inspection 590909 - Tropicana Products, Inc. - 2009-06-22](https://www.globalkeysolutions.net/records/fda_inspections/tropicana-products-inc/09a0724c-caaa-43e4-895f-3e7887c5283f) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2009

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