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FDA Inspection
•Glaropharm Ag•June 15, 2018

Glaropharm Ag – FDA Inspection, Jun 15, 2018

Record Details

This FDA Inspection record concerns Glaropharm Ag, with an inspection on June 15, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Glaropharm Ag
Inspection Date
June 15, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Sandra A. Boyd (Investigator)
View Company Profile

ID · 2830e9fa-e332-4204-a292-1d8a08967fef

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1058998
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Glaropharm Ag

1
DateClassificationOfficeProject area
May 31, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Glaropharm Ag
  • FDA Inspection 1207105 - 2023-05-31

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