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483
•Avista Pharma Solutions, Inc.•July 25, 2025

Avista Pharma Solutions, Inc. – FDA 483, Jul 25, 2025

Record Details

Avista Pharma Solutions, Inc. in Agawam, MA, was inspected and cited for multiple deficiencies related to quality control, facility maintenance, and computer system controls. The inspection revealed failures to investigate environmental monitoring discrepancies, maintain clean and repaired facilities, adhere to quality unit procedures for environmental monitoring data approval, and implement adequate computer system access controls. These issues indicate significant concerns regarding the firm's adherence to cGMPs in its drug product sterility and endotoxin testing operations.

Company
Avista Pharma Solutions, Inc.
Inspection date
July 25, 2025
Product type
drugs
Office
New England District Office
People
  • Daniel L. Zheng (M.S., Consumer Safety Officer at FDA)
  • Ifechimere I. Okafor (investigator)
View Company Profile

ID · dda545e9-7e67-4c8e-a7de-c638725bd84e

Other documents for Avista Pharma Solutions, Inc.
  • EIR - 2025-07-25July 25, 2025
  • EIR - 2019-12-18December 18, 2019
  • 483 - 2013-09-27September 27, 2013

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