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FDA Inspection
•Abbvie SRL•November 21, 2017

Abbvie SRL – FDA Inspection, Nov 21, 2017

Record Details

This FDA Inspection record concerns Abbvie SRL, with an inspection on November 21, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Abbvie SRL
Inspection Date
November 21, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Catherine J. Laufmann (Investigator)
  • Saied A. Asbagh (FDA Associated Person)
View Company Profile

ID · f24db6ff-c132-4f05-94ff-730ff81c399b

Inspection Facts

Inspection number
1031720
FDA center
Human Drugs
Project area
New Drug Evaluation
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.198(a)Complaint Handling Procedure

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Abbvie SRL

5
DateClassificationOfficeProject area
May 20, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 15, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
October 9, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 5, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 11, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Abbvie SRL
  • FDA Inspection 1194457 - 2022-05-20
  • FDA Inspection 1075266 - 2018-11-15
  • FDA Inspection 947575 - 2015-10-09
  • FDA Inspection 897973 - 2014-09-05
  • FDA Inspection 597617 - 2009-06-11

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