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 3005734706.
Observations2
Issue DateFebruary 28, 2017
Status1 Related Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections3
Establishment Details
Firm
MasterPharm LLC
Location
South Richmond Hill, New York, United States
FEI Number
3005734706
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
February 28, 2017
Country
United States
Inspection History, 2015 to 2020
VAI1
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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