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FDA Inspection
•Exelead, Inc.•December 20, 2023

Exelead, Inc. – FDA Inspection, Dec 20, 2023

Record Details

This FDA Inspection record concerns Exelead, Inc., with an inspection on December 20, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Exelead, Inc.
Inspection Date
December 20, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Lisa L. Flores (Investigator)
  • Muna Algharibeh (FDA Associated Person)
View Company Profile

ID · f8900203-7a73-476a-a795-450d85e7698c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1225603
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Exelead, Inc.

11
DateClassificationOfficeProject area
September 4, 2025Not classifiedDetroit District Office
July 30, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 15, 2018Not classifiedDetroit District Office
April 10, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 16, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 11 other inspections on the company page
Other documents for Exelead, Inc.
  • FDA Inspection 1287394 - 2025-09-04
  • FDA Inspection 1062147 - 2018-07-30
  • FDA Inspection 1055813 - 2018-05-15
  • FDA Inspection 922118 - 2015-04-10
  • FDA Inspection 878732 - 2014-05-16

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