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FDA Inspection 1029942 — CorePharma, LLC

CorePharma, LLC — FEI 3002535019

The FDA completed an inspection of CorePharma, LLC on October 13, 2017 in Middlesex, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 13, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Middlesex, NJ (United States)

Facility

Other inspections at this facility

  • 1280399 (NAI Thu Aug 28 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1240419 (NAI Thu Sep 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1087306 (NAI Fri Mar 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980585 (NAI Thu Aug 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 915404 (NAI Tue Feb 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources