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483
•Dhaliwal Pharmaceuticals Laboratories, LLC•March 1, 2022

Dhaliwal Pharmaceuticals Laboratories, LLC – FDA 483, Mar 1, 2022

Record Details

Dhaliwal Pharmaceuticals Laboratories, LLC, an OTC drug manufacturer in Mesquite, TX, was cited for failing to follow written production and process control procedures. Specifically, the firm had not completed process validation studies for an OTC topical drug product, leading to the release of unvalidated batches. This indicates a significant lapse in quality control and adherence to manufacturing standards.

Company
Dhaliwal Pharmaceuticals Laboratories, LLC
Inspection date
March 1, 2022
Product type
drugs
Office
Division of Human and Animal Food Operations - West III
Person
  • Michelle A. Krayer
View Company Profile

ID · 966efe70-32ac-40c8-8ed4-e9f8a2f9337b

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