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FDA Inspection
•ChemRite CoPac LLC•April 11, 2023

ChemRite CoPac LLC – FDA Inspection, Apr 11, 2023

Record Details

This FDA Inspection record concerns ChemRite CoPac LLC, with an inspection on April 11, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
ChemRite CoPac LLC
Inspection Date
April 11, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Michele L. Glendenning (FDA Associated Person)
  • Soyinka S. Eneng (Issuing Officer)
View Company Profile

ID · 39b1b1c5-482a-4c8e-bf86-7c65a268cfd1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1204584
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of ChemRite CoPac LLC

6
DateClassificationOfficeProject area
September 18, 2026Not classifiedMinneapolis District OfficeDrug Quality Assurance
July 15, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 24, 2016VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
February 21, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 21, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for ChemRite CoPac LLC
  • FDA Inspection 1336320 - 2026-09-18
  • FDA Inspection 987532 - 2016-07-15
  • FDA Inspection 971375 - 2016-03-24
  • FDA Inspection 820373 - 2013-02-21
  • FDA Inspection 756820 - 2011-11-21

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