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FDA Inspection 1085673 — ARx LLC

ARx LLC — FEI 2528933

The FDA completed an inspection of ARx LLC on March 29, 2019 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
March 29, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Glen Rock, PA (United States)

Facility

Other inspections at this facility

  • 1170966 (VAI Fri Jun 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1151907 (NAI Fri Aug 20 2021 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))
  • 737192 (NAI Fri Jul 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources