# Tam Fresh Cut-Pak Inc, Sacramento, CA – FDA Inspections

Source: https://www.keypedia.com/companies/tam-fresh-cut-pak-inc/a529ffb3-8fa5-4d76-a5d9-678b14d51a84

> Inspection records and compliance data for Tam Fresh Cut-Pak Inc in Sacramento, California. 6 FDA inspections on record, 1 Form 483, last inspected January 31, 2025.

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## Details

- Name: Tam Fresh Cut-Pak Inc
- FEI Number: 1000522866
- Address Line 1: 6400 Belleau Wood Ln Ste 1-2
- City: Sacramento
- State: California
- Zip Code: 95822
- Country Name: United States
- Address: 6400 Belleau Wood Ln Ste 1-2, Sacramento, California 95822, United States
- Country: United States

## Related Documents

- FDA Inspection 1260220 - Tam Fresh Cut-Pak Inc - 2025-01-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1260220 - Tam Fresh Cut-Pak Inc - 2025-01-31](https://www.keypedia.com/records/fda_inspections/tam-fresh-cut-pak-inc/d81d87e3-fa5a-4472-94e9-1eb89871e97f) — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2025
- FDA Inspection 1260220 - Tam Fresh Cut-Pak Inc - 2025-01-31 — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1166358 - Tam Fresh Cut-Pak Inc - 2022-03-24](https://www.keypedia.com/records/fda_inspections/tam-fresh-cut-pak-inc/c4be4b26-7710-4258-9a5f-8a47f35bdb98) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2022
- FDA Inspection 1131627 - Tam Fresh Cut-Pak Inc - 2020-09-17 — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2020
- FDA Inspection 1038716 - Tam Fresh Cut-Pak Inc - 2018-01-04 — source: FDA, date: January 4, 2018
- [FDA Inspection 912355 - Tam Fresh Cut-Pak Inc - 2015-01-21](https://www.keypedia.com/records/fda_inspections/tam-fresh-cut-pak-inc/76aab0ef-1e5c-4d4a-9af9-380137cbd0e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2015
- FDA Inspection 792447 - Tam Fresh Cut-Pak Inc - 2012-06-28 — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2012

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