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FDA Inspection
•Reliance Private Label Supplements•August 3, 2010

Reliance Private Label Supplements – FDA Inspection, Aug 3, 2010

Record Details

This FDA Inspection record concerns Reliance Private Label Supplements, with an inspection on August 3, 2010, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Reliance Private Label Supplements
Inspection Date
August 3, 2010
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 2937e802-6116-4cc6-86fc-c0012c6db631

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
674270
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

7
  1. 21 CFR 111.180(b)(3)(i)Document - required operation
  2. 21 CFR 111.570(b)(2)(i)Record - person document; time of performance
  3. 21 CFR 111.303Written procedures - tests, examinations; specifications met
  4. 21 CFR 111.14(b)(2)Personnel - records - training
  5. 21 CFR 111.415(b)Dietary supplement - protect, contamination
  6. 21 CFR 111.560(b)Quality control, review, approve; investigate, follow-up
  7. 21 CFR 111.465(a)(2)Hold - reserve sample; closure system

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Reliance Private Label Supplements

5
DateClassificationOfficeProject area
September 16, 2025Not classifiedNew Jersey District Office
June 29, 2018NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 28, 2015NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 28, 2015NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
April 20, 2009NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
Other documents for Reliance Private Label Supplements
  • FDA Inspection 1250588 - 2025-09-16
  • FDA Inspection 1059777 - 2018-06-29
  • FDA Inspection 943978 - 2015-09-28
  • FDA Inspection 943977 - 2015-09-28
  • FDA Inspection 577101 - 2009-04-20

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