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FDA Inspection 700587 — ARx LLC

ARx LLC — FEI 2528933

The FDA completed an inspection of ARx LLC on December 3, 2010 in Glen Rock, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 3, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glen Rock, PA (United States)

Facility

Other inspections at this facility

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  • 1151907 (NAI Fri Aug 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1085673 (VAI Fri Mar 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988507 (NAI Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867422 (NAI Tue Feb 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources