Source: FDA, document withdrawn. FDA released the Form 483 for this inspection and has since taken the document down, so there is nothing left to link to. The inspection itself is still FDA's published record, and a FOIA request is the way to ask for the form. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3010078541.
Observations1
Issue DateJuly 10, 2015
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Talk to a Specialist