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FDA Inspection
•KBI Biopharma, Inc.•April 1, 2026

KBI Biopharma, Inc. – FDA Inspection, Apr 1, 2026

Record Details

This FDA Inspection record concerns KBI Biopharma, Inc., with an inspection on April 1, 2026, issued by the Atlanta District Office, covering human drugs.

Company
KBI Biopharma, Inc.
Inspection Date
April 1, 2026
Product Type
Human Drugs
Office
Atlanta District Office
People
  • Marian E. Ramirez (Company Rep)
  • Yoriann M. Cabrera Bartolomei (Issuing Officer)
View Company Profile

ID · c23fd1bf-6113-4a1b-956d-885f190a4130

Inspection Facts

Inspection number
1312108
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of KBI Biopharma, Inc.

5
DateClassificationOfficeProject area
June 18, 2024Not classifiedAtlanta District Office
April 11, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 16, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 29, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 9, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for KBI Biopharma, Inc.
  • FDA Inspection 1241524 - 2024-06-18
  • FDA Inspection 1051652 - 2018-04-11
  • FDA Inspection 937768 - 2015-07-16
  • FDA Inspection 796226 - 2012-08-29
  • FDA Inspection 625271 - 2009-10-09

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