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483
•Ash Stevens LLC•July 9, 2009

Ash Stevens LLC – FDA 483, Jul 9, 2009

Record Details

An FDA inspection of Ash Stevens Inc. in Riverview, MI, revealed two significant observations related to their API manufacturing operations. The firm failed to implement adequate procedures for handling approved solvents during dispensing, posing a risk of cross-contamination. Additionally, written procedures for the preventative maintenance of production equipment were not followed, resulting in missing and incomplete documentation.

Company
Ash Stevens LLC
Inspection date
July 9, 2009
Product type
drugs
Office
Division of Pharmaceutical Quality Operations III
Person
  • Caroline H. Le (Investigator)
View Company Profile

ID · 1605c765-13c5-46ed-bafa-96a3bebfa97a

Other documents for Ash Stevens LLC
  • EIR - 2022-11-04November 4, 2022
  • EIR - 2015-11-02November 2, 2015
  • 483 - 2010-12-22December 22, 2010
  • 483 - 2004-11-04November 4, 2004
  • 483 - 2000-12-06December 6, 2000

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