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483
•FreshPoint Denver, Incorporated•December 15, 2025

FreshPoint Denver, Incorporated – FDA 483, Dec 15, 2025

Record Details

An FDA inspection of FreshPoint Denver, Incorporated in Denver, CO, revealed an issue with inadequate sanitary facilities. Specifically, a y-splitter/hose connector valve was found under continuous pressure without proper backflow protection, posing a risk of contamination to the internal water supply. This indicates a significant concern regarding the firm's sanitation practices.

Company
FreshPoint Denver, Incorporated
Inspection date
December 15, 2025
Product type
other
Office
Denver District Office
Person
  • Megan K. Rand
View Company Profile

ID · ff1bd629-4ecb-4391-9f1d-7ea0acfde960

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