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483
•Pacira Pharmaceuticals, Inc.•July 22, 2015

Pacira Pharmaceuticals, Inc. – FDA 483, Jul 22, 2015

Record Details

An FDA inspection of Pacira Pharmaceuticals, Inc. in San Diego, CA, a drug manufacturer, revealed significant deficiencies across its facilities, equipment, production, and laboratory control systems. The firm failed to adequately maintain and qualify equipment, lacked proper cleaning procedures for stability chambers, and exhibited shortcomings in its investigation of discrepancies and documentation practices. These issues indicate a lack of adherence to current Good Manufacturing Practices, potentially impacting drug product quality and safety.

Company
Pacira Pharmaceuticals, Inc.
Inspection date
July 22, 2015
Product type
drugs
Office
Division of Pharmaceutical Quality Operations IV
People
  • Theresa Kirkham
  • Paul A. Bonneau (Chef de projet)
  • Virgilio F. Pacio (investigator)
View Company Profile

ID · 57b5b6fb-1fd8-46b9-aa4d-73aa4e0ef8c5

Other documents for Pacira Pharmaceuticals, Inc.
  • 483 - 2023-04-19April 19, 2023
  • 483 - 2018-03-01March 1, 2018
  • EIR - 2018-03-01March 1, 2018

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