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 3011838368.
Observations1
Issue DateFebruary 14, 2019
StatusNo Warning Letter
Establishment TypeProducer of Non Sterile Drug Products
Related Inspections0
Establishment Details
Firm
Buderer Drug Company
Location
Ohio, United States
FEI Number
3011838368
Establishment Type
Producer of Non Sterile Drug Products
Product Type
Drugs
Issue Date
February 14, 2019
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.
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