Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3002535019.
Observations2
Issue DateSeptember 14, 2009
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
CorePharma, LLC
Location
Middlesex, New Jersey, United States
FEI Number
3002535019
Product Type
Drugs
Issue Date
September 14, 2009
Country
United States
Inspection History, 2012 to 2025
NAI8
VAI1
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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