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FDA Inspection
•Lex, Inc.•February 28, 2023

Lex, Inc. – FDA Inspection, Feb 28, 2023

Record Details

This FDA Inspection record concerns Lex, Inc., with an inspection on February 28, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Lex, Inc.
Inspection Date
February 28, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Benita C. Okeke (Issuing Officer)
  • Nicole E. Knowlton (FDA Associated Person)
  • Suzanne N. Vallez (FDA Associated Person)
View Company Profile

ID · b888688d-350f-4780-af49-2b89f88a2b7f

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1200033
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Lex, Inc.

6
DateClassificationOfficeProject area
February 14, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 20, 2016VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
September 16, 2013VAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
March 1, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2010NAICenter for Food Safety and Applied NutritionFood Composition, Standards, Labeling and Econ
View all 6 other inspections on the company page
Other documents for Lex, Inc.
  • FDA Inspection 1041092 - 2018-02-14
  • FDA Inspection 958207 - 2016-01-20
  • FDA Inspection 848516 - 2013-09-16
  • FDA Inspection 707801 - 2011-03-01
  • FDA Inspection 680451 - 2010-09-28

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Contact
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Scranton, PA, 18503
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