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FDA Inspection
•ByHeart Inc dba Blendhouse Allerton•January 22, 2026

ByHeart Inc dba Blendhouse Allerton – FDA Inspection, Jan 22, 2026

Record Details

This FDA Inspection record concerns ByHeart Inc dba Blendhouse Allerton, with an inspection on January 22, 2026, issued by the Kansas City District Office, covering foods & cosmetics.

Company
ByHeart Inc dba Blendhouse Allerton
Inspection Date
January 22, 2026
Product Type
Foods & Cosmetics
Office
Kansas City District Office
People
  • Danny Tuntevski (FDA Associated Person)
  • Karen M. Labounty (FDA Associated Person)
View Company Profile

ID · 78d0b154-5d16-43f5-a8c3-c1ddd9a8a315

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1291804
FDA center
Foods & Cosmetics
Project area
Foodborne Biological Hazards
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 106.30(b)Equipment, utensil - clean, sanitize
  2. 21 CFR 106.50(a)(1)Deviation from master order - investigation, corrections
  3. 21 CFR 106.6(c)(4)Review, evaluate deviation from specification

Full citation text and observation details available on the Dashboard.

Other FDA inspections of ByHeart Inc dba Blendhouse Allerton

16
DateClassificationOfficeProject area
February 20, 2025VAIKansas City District OfficeFoodborne Biological Hazards
January 30, 2024NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
June 28, 2023NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
June 30, 2022VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
January 15, 2020NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
View all 16 other inspections on the company page
Other documents for ByHeart Inc dba Blendhouse Allerton
  • FDA Inspection 1259414 - 2025-02-20
  • FDA Inspection 1230696 - 2024-01-30
  • FDA Inspection 1214825 - 2023-06-28
  • FDA Inspection 1173584 - 2022-06-30
  • FDA Inspection 1117456 - 2020-01-15

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