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FDA Inspection
•Opocrin SPA•May 6, 2016

Opocrin SPA – FDA Inspection, May 6, 2016

Record Details

This FDA Inspection record concerns Opocrin SPA, with an inspection on May 6, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Opocrin SPA
Inspection Date
May 6, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 39bc51a8-58f1-411f-bfab-244c92988c00

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
970807
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Opocrin SPA

2
DateClassificationOfficeProject area
February 25, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 29, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Opocrin SPA
  • FDA Inspection 1169545 - 2022-02-25
  • FDA Inspection 1092538 - 2017-09-29

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