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FDA Inspection
•Vee Pak, LLC•December 10, 2024

Vee Pak, LLC – FDA Inspection, Dec 10, 2024

Record Details

This FDA Inspection record concerns Vee Pak, LLC, with an inspection on December 10, 2024, issued by the Chicago District Office, covering human drugs.

Company
Vee Pak, LLC
Inspection Date
December 10, 2024
Product Type
Human Drugs
Office
Chicago District Office
People
  • Angela C. Welker (Issuing Officer)
  • Jean Claude Garay (Issuing Officer)
  • Michael A. Charles (FDA Associated Person)
View Company Profile

ID · c1005175-09a2-4516-97cd-121b26828642

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1255686
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.192Written record of investigation incomplete

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Vee Pak, LLC

3
DateClassificationOfficeProject area
April 5, 2017NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
June 17, 2015NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
June 21, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Vee Pak, LLC
  • FDA Inspection 1028656 - 2017-04-05
  • FDA Inspection 932391 - 2015-06-17
  • FDA Inspection 730598 - 2011-06-21

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