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FDA Inspection 890789 — CorePharma, LLC

CorePharma, LLC — FEI 3002535019

The FDA completed an inspection of CorePharma, LLC on August 12, 2014 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
August 12, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Middlesex, NJ (United States)

Facility

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  • 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))
  • 1029942 (NAI Fri Oct 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 980585 (NAI Thu Aug 11 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources