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FDA Inspection
•GH Genhelix S.A.•December 12, 2019

GH Genhelix S.A. – FDA Inspection, Dec 12, 2019

Record Details

This FDA Inspection record concerns GH Genhelix S.A., with an inspection on December 12, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
GH Genhelix S.A.
Inspection Date
December 12, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · cc7e9e5c-8eef-4b25-8d70-9aad3e0084b8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1202723
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of GH Genhelix S.A.

1
DateClassificationOfficeProject area
October 26, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for GH Genhelix S.A.
  • FDA Inspection 1276827 - 2022-10-26

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