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FDA Inspection
•United Laboratories Manufacturing, LLC•April 9, 2018

United Laboratories Manufacturing, LLC – FDA Inspection, Apr 9, 2018

Record Details

This FDA Inspection record concerns United Laboratories Manufacturing, LLC, with an inspection on April 9, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
United Laboratories Manufacturing, LLC
Inspection Date
April 9, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Nimmy Mathews (FDA Associated Person)
  • Shelby N. Turner (Investigator)
View Company Profile

ID · 8804f5ff-8284-4191-b651-0b64eb9b284b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1047444
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of United Laboratories Manufacturing, LLC

6
DateClassificationOfficeProject area
August 15, 2025VAIDallas District OfficeDrug Quality Assurance
March 7, 2025Not classifiedDallas District Office
May 9, 2023NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
August 26, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 16, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for United Laboratories Manufacturing, LLC
  • FDA Inspection 1251234 - 2025-08-15
  • FDA Inspection 1255830 - 2025-03-07
  • FDA Inspection 1208568 - 2023-05-09
  • FDA Inspection 987414 - 2016-08-26
  • FDA Inspection 796232 - 2012-08-16

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