# Kendall Juice Corporation, Hialeah, FL – FDA Inspections

Source: https://www.keypedia.com/companies/kendall-juice-corporation/eea955de-b53a-44d9-b06a-bf7b8ca5f89f

> Inspection records and compliance data for Kendall Juice Corporation in Hialeah, Florida. 4 FDA inspections on record, 4 Form 483s, last inspected February 09, 2026.

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## Details

- Name: Kendall Juice Corporation
- FEI Number: 3007957863
- Address Line 1: 4675 E 10th Ct
- City: Hialeah
- State: Florida
- Zip Code: 33013
- Country Name: United States
- Address: 4675 E 10th Ct, Hialeah, Florida 33013, United States
- Country: United States

## Related Documents

- [FDA Inspection 1301938 - Kendall Juice Corporation - 2026-02-09](https://www.keypedia.com/records/fda_inspections/kendall-juice-corporation/fa750ed1-4329-416d-a0e9-2581df341f07) — source: FDA, date: February 9, 2026
- FDA Inspection 1253960 - Kendall Juice Corporation - 2024-11-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2024
- [FDA Inspection 1253960 - Kendall Juice Corporation - 2024-11-13](https://www.keypedia.com/records/fda_inspections/kendall-juice-corporation/43643bfd-e077-4662-9133-228ed3077207) — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2024
- FDA Inspection 1253960 - Kendall Juice Corporation - 2024-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2024
- [FDA Inspection 1215107 - Kendall Juice Corporation - 2023-08-18](https://www.keypedia.com/records/fda_inspections/kendall-juice-corporation/a92c52d7-f23c-4e54-a563-4c04131ad20e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2023
- FDA Inspection 1215107 - Kendall Juice Corporation - 2023-08-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2023
- [FDA Inspection 1056264 - Kendall Juice Corporation - 2018-06-18](https://www.keypedia.com/records/fda_inspections/kendall-juice-corporation/8925b65c-fc3b-45d5-8b1c-b656ddf08305) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 18, 2018

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