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FDA Inspection
•Nartex Laboratorios Homeopaticos S.A. de C.V.•December 15, 2023

Nartex Laboratorios Homeopaticos S.A. de C.V. – FDA Inspection, Dec 15, 2023

Record Details

This FDA Inspection record concerns Nartex Laboratorios Homeopaticos S.A. de C.V., with an inspection on December 15, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Nartex Laboratorios Homeopaticos S.A. de C.V.
Inspection Date
December 15, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Alan M. Barker (FDA Associated Person)
  • Jose M. Cayuela (FDA Associated Person)
View Company Profile

ID · 831b6972-2ff1-448c-ad2f-7140f65208ce

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1228195
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Nartex Laboratorios Homeopaticos S.A. de C.V.

1
DateClassificationOfficeProject area
February 28, 2020OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Nartex Laboratorios Homeopaticos S.A. de C.V.
  • FDA Inspection 1123300 - 2020-02-28

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