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FDA Inspection
•Procos S.p.A.•May 19, 2017

Procos S.p.A. – FDA Inspection, May 19, 2017

Record Details

This FDA Inspection record concerns Procos S.p.A., with an inspection on May 19, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Procos S.p.A.
Inspection Date
May 19, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Unnee Ranjan (FDA Associated Person)
View Company Profile

ID · 26b2a924-0bc8-4797-a4eb-24a3ba6c4d80

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1014777
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Procos S.p.A.

5
DateClassificationOfficeProject area
September 16, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 1, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 26, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 1, 2013NAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
May 19, 2010VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Procos S.p.A.
  • FDA Inspection 1243875 - 2022-09-16
  • FDA Inspection 1098744 - 2019-02-01
  • FDA Inspection 964517 - 2016-02-26
  • FDA Inspection 842649 - 2013-08-01
  • FDA Inspection 667150 - 2010-05-19

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