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FDA Inspection
•QualTech Laboratories, Inc.•April 13, 2026

QualTech Laboratories, Inc. – FDA Inspection, Apr 13, 2026

Record Details

This FDA Inspection record concerns QualTech Laboratories, Inc., with an inspection on April 13, 2026, issued by the New Jersey District Office, covering human drugs.

Company
QualTech Laboratories, Inc.
Inspection Date
April 13, 2026
Product Type
Human Drugs
Office
New Jersey District Office
Person
  • Frederick Razzaghi (FDA Associated Person)
View Company Profile

ID · cbee1ea6-8ecf-4feb-bcd7-a2a8a4e335ff

Inspection Facts

Inspection number
1314634
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.194(a)(1)Sample identification and other information

Full citation text and observation details available on the Dashboard.

Other FDA inspections of QualTech Laboratories, Inc.

7
DateClassificationOfficeProject area
October 25, 2022NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 11, 2018NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
May 12, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 19, 2014NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
April 8, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for QualTech Laboratories, Inc.
  • FDA Inspection 1187441 - 2022-10-25
  • FDA Inspection 1040300 - 2018-01-11
  • FDA Inspection 971475 - 2016-05-12
  • FDA Inspection 903571 - 2014-11-19
  • FDA Inspection 826421 - 2013-04-08

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