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The process: 2003-2006
nEstablish
a provisional process by which Category IIIA
products will be reclassified and implement the process
nPublish
a Proposed Order – Federal Register
nFDA’s reclassification of IIIA
products into Category I or II
nPeriod
for public comment after issuance of Proposed Order
nConsider
public responses, and revise order as necessary
nPublish
a Final Order – Federal
Register
nClassification
nRevoke
licenses for products reclassified into Category II