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FDA Inspection
•Immunex Rhode Island Corporation•April 19, 2019

Immunex Rhode Island Corporation – FDA Inspection, Apr 19, 2019

Record Details

This FDA Inspection record concerns Immunex Rhode Island Corporation, with an inspection on April 19, 2019, issued by the New England District Office, covering human drugs.

Company
Immunex Rhode Island Corporation
Inspection Date
April 19, 2019
Product Type
Human Drugs
Office
New England District Office
People
  • Zhihao Pete Qiu (Issuing Officer)
  • Ziyang Su (Issuing Officer)
View Company Profile

ID · 63b1dd6a-fb06-4ab8-bf3c-1b983b24e522

Inspection Facts

Inspection number
1092675
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Immunex Rhode Island Corporation

8
DateClassificationOfficeProject area
June 3, 2026Not classifiedNew England District Office
October 27, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 2, 2018Not classifiedNew England District Office
July 17, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 3, 2017Not classifiedNew England District Office
View all 8 other inspections on the company page
Other documents for Immunex Rhode Island Corporation
  • FDA Inspection 1324094 - 2026-06-03
  • FDA Inspection 1191233 - 2022-10-27
  • FDA Inspection 1071184 - 2018-11-02
  • FDA Inspection 1028526 - 2017-07-17
  • FDA Inspection 1000373 - 2017-02-03

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