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FDA Inspection
•Cambrex Profarmaco Milano Srl•May 19, 2017

Cambrex Profarmaco Milano Srl – FDA Inspection, May 19, 2017

Record Details

This FDA Inspection record concerns Cambrex Profarmaco Milano Srl, with an inspection on May 19, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Cambrex Profarmaco Milano Srl
Inspection Date
May 19, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Margaret M. Annes (FDA Associated Person)
  • Temar Q. Williams
View Company Profile

ID · 66ac1960-e277-4a92-bdb1-667be3edb250

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1021644
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Cambrex Profarmaco Milano Srl

7
DateClassificationOfficeProject area
November 11, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 1, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 7, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 6, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 6, 2013NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
View all 7 other inspections on the company page
Other documents for Cambrex Profarmaco Milano Srl
  • FDA Inspection 1193220 - 2022-11-11
  • FDA Inspection 1167505 - 2021-10-01
  • FDA Inspection 1091698 - 2019-05-07
  • FDA Inspection 973972 - 2015-11-06
  • FDA Inspection 861141 - 2013-12-06

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