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FDA Inspection
•Quality Chemical Laboratories•July 27, 2017

Quality Chemical Laboratories – FDA Inspection, Jul 27, 2017

Record Details

This FDA Inspection record concerns Quality Chemical Laboratories, with an inspection on July 27, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Quality Chemical Laboratories
Inspection Date
July 27, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Kara D. Dobbin (Issuing Officer)
  • Tajah L. Blackburn (FDA Associated Person)
View Company Profile

ID · 05d68d67-387f-438f-9622-8917dd74cef0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1020031
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 211.22(d)Procedures not in writing, fully followed
  2. 21 CFR 211.100(b)SOPs not followed / documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Quality Chemical Laboratories

6
DateClassificationOfficeProject area
July 24, 2025NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 20, 2024VAIAtlanta District OfficeDrug Quality Assurance
June 21, 2016NAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
September 26, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 24, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Quality Chemical Laboratories
  • FDA Inspection 1281246 - 2025-07-24
  • FDA Inspection 1254678 - 2024-11-20
  • FDA Inspection 984876 - 2016-06-21
  • FDA Inspection 850707 - 2013-09-26
  • FDA Inspection 681412 - 2010-08-24

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