Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3011761882.
Observations3
Issue DateSeptember 09, 2022
Status1 Related Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections4
Establishment Details
Firm
Curexa - East, LLC dba Curexa
Location
Egg Harbor Township, New Jersey, United States
FEI Number
3011761882
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
September 09, 2022
Country
United States
Inspection History, 2018 to 2026
NAI1
VAI2
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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