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483
•Avista Pharma Solutions, Inc.•September 27, 2013

Avista Pharma Solutions, Inc. – FDA 483, Sep 27, 2013

Record Details

Microtest Laboratories, Inc. in Agawam, MA, was inspected by the FDA from September 16-27, 2013, and received eight observations. The inspection revealed significant deficiencies in quality control, aseptic processing, environmental monitoring, and validation of sterile drug product manufacturing. Key issues include releasing sterile injectable products without complete testing, inadequate smoke studies, and failures in investigating discrepancies and validating sterilization processes.

Company
Avista Pharma Solutions, Inc.
Inspection date
September 27, 2013
Product type
biologics
Office
Division of Northeast Imports 
Person
  • Maya M. Davis (Assuring that quality medicines are available to the American public)
View Company Profile

ID · 9f9dbbb7-e4b8-44a3-81c1-7d55709ef9c2

Other documents for Avista Pharma Solutions, Inc.
  • 483 - 2025-07-25July 25, 2025
  • EIR - 2025-07-25July 25, 2025
  • EIR - 2019-12-18December 18, 2019

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