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FDA Inspection
•GREFI•April 5, 2018

GREFI – FDA Inspection, Apr 5, 2018

Record Details

This FDA Inspection record concerns GREFI, with an inspection on April 5, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
GREFI
Inspection Date
April 5, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Laura E. Garcia (Issuing Officer)
View Company Profile

ID · 63befdfa-b892-4a51-a280-f62023950dfc

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1048379
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 1271.47(a)Procedures for all other requirements
  2. 21 CFR 1271.85(a)Infection with communicable disease agents

Full citation text and observation details available on the Dashboard.

Other FDA inspections of GREFI

3
DateClassificationOfficeProject area
June 14, 2021OAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
October 1, 2019OAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 31, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for GREFI
  • FDA Inspection 1145211 - 2021-06-14
  • FDA Inspection 1101917 - 2019-10-01
  • FDA Inspection 941188 - 2015-08-31

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