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FDA Inspection
•Grifols Therapeutics LLC•December 13, 2018

Grifols Therapeutics LLC – FDA Inspection, Dec 13, 2018

Record Details

This FDA Inspection record concerns Grifols Therapeutics LLC, with an inspection on December 13, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Grifols Therapeutics LLC
Inspection Date
December 13, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Cynthia Jim (FDA Associated Person)
View Company Profile

ID · a8c4df93-a1d3-415f-a6ee-5067a6f6675c

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1079999
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of Grifols Therapeutics LLC

8
DateClassificationOfficeProject area
February 5, 2026Not classifiedAtlanta District OfficeBlood and Blood Products
September 1, 2023Not classifiedAtlanta District Office
May 6, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
February 10, 2017Not classifiedAtlanta District Office
October 21, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 8 other inspections on the company page
Other documents for Grifols Therapeutics LLC
  • FDA Inspection 1302186 - 2026-02-05
  • FDA Inspection 1221101 - 2023-09-01
  • FDA Inspection 1176467 - 2022-05-06
  • FDA Inspection 1003199 - 2017-02-10
  • FDA Inspection 994781 - 2016-10-21

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