# Alpine Fresh, LLC, Doral, FL – FDA Inspections

Source: https://www.keypedia.com/companies/alpine-fresh-llc/277e7925-35c5-442b-9fa8-7b151da2da74

> Inspection records and compliance data for Alpine Fresh, LLC in Doral, Florida. 6 FDA inspections on record, 1 Form 483, last inspected September 16, 2026.

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## Details

- Name: Alpine Fresh, LLC
- FEI Number: 1000151158
- Address Line 1: 9300 Nw 58th St Ste 201
- City: Doral
- State: Florida
- Zip Code: 33178
- Country Name: United States
- Address: 9300 Nw 58th St Ste 201, Doral, Florida 33178, United States
- Country: United States

## Related Documents

- FDA Inspection 1332606 - Alpine Fresh, LLC - 2026-09-16 — classification: No Action Indicated (NAI), source: FDA, date: September 16, 2026
- FDA Inspection 1319438 - Alpine Fresh, LLC - 2026-05-11 — classification: No Action Indicated (NAI), source: FDA, date: May 11, 2026
- [FDA Inspection 1242343 - Alpine Fresh, LLC - 2024-06-25](https://www.keypedia.com/records/fda_inspections/alpine-fresh-llc/3d5eb9f4-bf5e-4b56-96ff-3ef4d6a5d491) — source: FDA, date: June 25, 2024
- FDA Inspection 1190314 - Alpine Fresh, LLC - 2022-11-08 — classification: No Action Indicated (NAI), source: FDA, date: November 8, 2022
- [FDA Inspection 1127732 - Alpine Fresh, LLC - 2020-08-26](https://www.keypedia.com/records/fda_inspections/alpine-fresh-llc/fe84c164-0c30-473f-8edf-f5b3d26a3da1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 26, 2020
- FDA Inspection 1100780 - Alpine Fresh, LLC - 2019-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2019
- FDA Inspection 1100780 - Alpine Fresh, LLC - 2019-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2019
- [FDA Inspection 1100780 - Alpine Fresh, LLC - 2019-08-08](https://www.keypedia.com/records/fda_inspections/alpine-fresh-llc/feef85fd-a894-4f65-a7f1-f292ce3872ff) — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2019
- FDA Inspection 1100780 - Alpine Fresh, LLC - 2019-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2019

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