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483
•Chartwell Pharmaceuticals Carmel LLC•February 28, 2018

Chartwell Pharmaceuticals Carmel LLC – FDA 483, Feb 28, 2018

Record Details

An FDA inspection of Silarx Pharmaceuticals, Inc. in Carmel, NY, a drug product manufacturer, revealed two significant observations. The firm failed to properly handle drug product complaints, specifically neglecting to investigate an adverse reaction report for Loratidine Oral Solution. Additionally, routine equipment checks, including temperature monitoring for critical storage units, were not performed according to a written program on weekends and non-operational days.

Company
Chartwell Pharmaceuticals Carmel LLC
Inspection date
February 28, 2018
Product type
drugs
Office
Division of Human and Animal Food Operations - East I
Person
  • Helen B. Ricalde (Director, Team Biologics Staff)
View Company Profile

ID · e2b1e4ee-6b51-46f3-99ec-d77208ad7557

Other documents for Chartwell Pharmaceuticals Carmel LLC
  • 483 - 2024-12-20December 20, 2024
  • 483 - 2024-01-11January 11, 2024
  • 483 - 2022-10-06October 6, 2022
  • 483 - 2019-12-16December 16, 2019
  • EIR - 2019-12-16December 16, 2019

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