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FDA Inspection
•Avon Manufacturing (Guangzhou) Ltd.•December 1, 2023

Avon Manufacturing (Guangzhou) Ltd. – FDA Inspection, Dec 1, 2023

Record Details

This FDA Inspection record concerns Avon Manufacturing (Guangzhou) Ltd., with an inspection on December 1, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Avon Manufacturing (Guangzhou) Ltd.
Inspection Date
December 1, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Wayne D. Mcgrath
View Company Profile

ID · a24dd6ad-605e-4fe3-8877-87b04c8a5f11

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1225519
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Avon Manufacturing (Guangzhou) Ltd.

2
DateClassificationOfficeProject area
June 7, 2018OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 7, 2014NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Avon Manufacturing (Guangzhou) Ltd.
  • FDA Inspection 1056501 - 2018-06-07
  • FDA Inspection 881720 - 2014-05-07

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