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I heard that FDA changed its emergency use authorization for the Influenza A H1N1 (2009) Real Time RT-PCR — why would the FDA do this?

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I heard that FDA changed its emergency use authorization for the Influenza A H1N1 (2009) Real Time RT-PCR — why would the FDA do this?

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On August 17, FDA issued an amended EUA for the Focus Diagnostics test. The EUA was amended to reflect labeling clarifications regarding the contents of the test kit.

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