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FDA Inspection
•Qualtex Laboratories•February 27, 2020

Qualtex Laboratories – FDA Inspection, Feb 27, 2020

Record Details

This FDA Inspection record concerns Qualtex Laboratories, with an inspection on February 27, 2020, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Qualtex Laboratories
Inspection Date
February 27, 2020
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · d09a3836-2931-410a-a224-e52552938160

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1122019
FDA center
Biologics
Project area
Vaccines and Allergenic Products

Other FDA inspections of Qualtex Laboratories

12
DateClassificationOfficeProject area
September 27, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 27, 2020NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 21, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 15, 2017VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 20, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 12 other inspections on the company page
Other documents for Qualtex Laboratories
  • FDA Inspection 1251335 - 2024-09-27
  • FDA Inspection 1122001 - 2020-02-27
  • FDA Inspection 1028892 - 2017-09-21
  • FDA Inspection 1025875 - 2017-09-15
  • FDA Inspection 939930 - 2015-08-20

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