Regulations.gov document

Response Letter from FDA CDER to Keryx Biopharmaceuticals, Inc.

Other · FDA-2018-P-3284 · posted Jan 31, 2019

Key facts

Document ID FDA-2018-P-3284-0022
Title Response Letter from FDA CDER to Keryx Biopharmaceuticals, Inc.
Document type Other
Subtype Agency Response
Agency FDA
Docket FDA-2018-P-3284
Posted Jan 31, 2019
Comment period opens Jan 31, 2019

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