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FDA Inspection
•Velocity Pharma LLC•January 26, 2012

Velocity Pharma LLC – FDA Inspection, Jan 26, 2012

Record Details

This FDA Inspection record concerns Velocity Pharma LLC, with an inspection on January 26, 2012, issued by the Center for Food Safety and Applied Nutrition, covering food/cosmetics.

Company
Velocity Pharma LLC
Inspection Date
January 26, 2012
Product Type
Food/cosmetics
Office
Center for Food Safety and Applied Nutrition
View Company Profile

ID · 34921975-9692-41eb-9162-c2921c0121c0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
762085
FDA center
Foods & Cosmetics
Project area
Food Composition, Standards, Labeling and Econ

FDA Citations

8
  1. 21 CFR 111.75(a)(2)Appropriate tests, examinations; certificate of analysis
  2. 21 CFR 111.453Written procedures - holding
  3. 21 CFR 111.503Written procedures - returned dietary supplement
  4. 21 CFR 111.415Fill, assemble, package, label - master record
  5. 21 CFR 111.430(b)Records - packaging, labeling operations
  6. 21 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
  7. 21 CFR 111.365Manufacturing operations - prevent contamination
  8. 21 CFR 111.75(c)Specifications met - verify; finished batch

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Velocity Pharma LLC

8
DateClassificationOfficeProject area
December 14, 2023OAIDrug Quality Assurance
October 23, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 7, 2019VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
May 18, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 17, 2014NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 8 other inspections on the company page
Other documents for Velocity Pharma LLC
  • FDA Inspection 1225060 - 2023-12-14
  • FDA Inspection 1131767 - 2020-10-23
  • FDA Inspection 1092199 - 2019-06-07
  • FDA Inspection 972342 - 2016-05-18
  • FDA Inspection 864122 - 2014-01-17

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