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FDA Inspection
•LFB USA, Inc.•May 12, 2017

LFB USA, Inc. – FDA Inspection, May 12, 2017

Record Details

This FDA Inspection record concerns LFB USA, Inc., with an inspection on May 12, 2017, issued by the New England District Office, covering biologics.

Company
LFB USA, Inc.
Inspection Date
May 12, 2017
Product Type
Biologics
Office
New England District Office
People
  • Deborah M. Trout (Issuing Officer)
  • Nicole M. Li (Issuing Officer)
View Company Profile

ID · 67f628c1-5036-46c3-ba14-a4c6492bad27

Inspection Facts

Inspection number
1028254
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of LFB USA, Inc.

3
DateClassificationOfficeProject area
June 28, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 8, 2022VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 22, 2017NAICenter for Veterinary MedicineBioresearch Monitoring
Other documents for LFB USA, Inc.
  • FDA Inspection 1244007 - 2024-06-28
  • FDA Inspection 1174664 - 2022-04-08
  • FDA Inspection 1039570 - 2017-08-22

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