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FDA Inspection
•Unilever Mexico S de R.L. de C.V.•September 7, 2017

Unilever Mexico S de R.L. de C.V. – FDA Inspection, Sep 7, 2017

Record Details

This FDA Inspection record concerns Unilever Mexico S de R.L. de C.V., with an inspection on September 7, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Unilever Mexico S de R.L. de C.V.
Inspection Date
September 7, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Rozelle G. Smith (Company Rep)
  • Vilmary Negron Rodriguez (Issuing Officer)
View Company Profile

ID · d8f834d1-204c-455f-9603-3a4c7615bb7c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1028607
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Unilever Mexico S de R.L. de C.V.

2
DateClassificationOfficeProject area
August 12, 2016NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
September 7, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Unilever Mexico S de R.L. de C.V.
  • FDA Inspection 992740 - 2016-08-12
  • FDA Inspection 750369 - 2011-09-07

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