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FDA Inspection
•RePharm LLC•November 15, 2023

RePharm LLC – FDA Inspection, Nov 15, 2023

Record Details

This FDA Inspection record concerns RePharm LLC, with an inspection on November 15, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
RePharm LLC
Inspection Date
November 15, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Gretchen L. Trendel (Issuing Officer)
View Company Profile

ID · d956da1e-9a08-4d15-acab-0d5131399560

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1224274
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of RePharm LLC

2
DateClassificationOfficeProject area
June 25, 2021OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 3, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for RePharm LLC
  • FDA Inspection 1145918 - 2021-06-25
  • FDA Inspection 1095778 - 2019-07-03

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