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FDA Inspection
•Grifols Biologicals LLC•August 24, 2017

Grifols Biologicals LLC – FDA Inspection, Aug 24, 2017

Record Details

This FDA Inspection record concerns Grifols Biologicals LLC, with an inspection on August 24, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Grifols Biologicals LLC
Inspection Date
August 24, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Gene D. Arcy
View Company Profile

ID · f25a02a9-3727-4b96-badb-2b0b7d911ebd

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1027351
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of Grifols Biologicals LLC

8
DateClassificationOfficeProject area
September 17, 2026Not classifiedLos Angeles District OfficeBlood and Blood Products
May 3, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 12, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 31, 2019Not classifiedLos Angeles District Office
October 20, 2015VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 8 other inspections on the company page
Other documents for Grifols Biologicals LLC
  • FDA Inspection 1336990 - 2026-09-17
  • FDA Inspection 1229139 - 2024-05-03
  • FDA Inspection 1105923 - 2019-09-12
  • FDA Inspection 1088286 - 2019-01-31
  • FDA Inspection 944819 - 2015-10-20

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