In case of receiving inquiries from SFDA about a medical device Field Safety Corrective Action that they received from more than one source, but for the company is considered as one Field Safety Notice should all of them be closed, or it should be reported that they are the same Field Safety Notice which was previously answered?
2024-02-20
SFDA must be informed of any duplicated Field Safety Notices and any updated information related to affected medical device or the corrective action.
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