# Sanwa Fresh Produce Co, Llc, Tampa, FL – FDA Inspections

Source: https://www.keypedia.com/companies/sanwa-fresh-produce-co-llc/3343aecc-49ea-4f23-ac08-51736af66b95

> Inspection records and compliance data for Sanwa Fresh Produce Co, Llc in Tampa, Florida. 6 FDA inspections on record, 1 Form 483, last inspected January 16, 2025.

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## Details

- Name: Sanwa Fresh Produce Co, Llc
- FEI Number: 3005092437
- Address Line 1: 2801 E Hillsborough Ave
- City: Tampa
- State: Florida
- Zip Code: 33610
- Country Name: United States
- Address: 2801 E Hillsborough Ave, Tampa, Florida 33610, United States
- Country: United States

## Related Documents

- [FDA Inspection 1258570 - Sanwa Fresh Produce Co, Llc - 2025-01-16](https://www.keypedia.com/records/fda_inspections/sanwa-fresh-produce-co-llc/dc676e12-ecb3-4960-b57e-3dd36b0e1b28) — source: FDA, date: January 16, 2025
- FDA Inspection 1006961 - Sanwa Fresh Produce Co, Llc - 2017-04-13 — source: FDA, date: April 13, 2017
- FDA Inspection 782593 - Sanwa Fresh Produce Co, Llc - 2012-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2012
- FDA Inspection 699539 - Sanwa Fresh Produce Co, Llc - 2010-11-29 — classification: No Action Indicated (NAI), source: FDA, date: November 29, 2010
- FDA Inspection 672431 - Sanwa Fresh Produce Co, Llc - 2010-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2010
- FDA Inspection 672431 - Sanwa Fresh Produce Co, Llc - 2010-06-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2010
- FDA Inspection 672431 - Sanwa Fresh Produce Co, Llc - 2010-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2010
- FDA Inspection 603147 - Sanwa Fresh Produce Co, Llc - 2009-07-10 — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2009
- FDA Inspection 603147 - Sanwa Fresh Produce Co, Llc - 2009-07-10 — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2009
- FDA Inspection 603147 - Sanwa Fresh Produce Co, Llc - 2009-07-10 — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2009

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