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FDA Inspection
•CELESTE INDUSTRIES CORPORATION•May 17, 2018

CELESTE INDUSTRIES CORPORATION – FDA Inspection, May 17, 2018

Record Details

This FDA Inspection record concerns CELESTE INDUSTRIES CORPORATION, with an inspection on May 17, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
CELESTE INDUSTRIES CORPORATION
Inspection Date
May 17, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Marcellinus D. Dordunoo (FDA Associated Person)
View Company Profile

ID · cb24944c-4502-4133-9753-8ed98082e79e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1057753
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of CELESTE INDUSTRIES CORPORATION

1
DateClassificationOfficeProject area
February 28, 2025VAIBaltimore District OfficeDrug Quality Assurance
Other documents for CELESTE INDUSTRIES CORPORATION
  • FDA Inspection 1262831 - 2025-02-28

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