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FDA Adverse Event Reports for AK Forte, Infla-650, and Umary
FDA Adverse Event Reports for AK Forte, Infla-650, and Umary
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Original Request: I am requesting copies of all adverse event reports submitted to the Food and Drug Administration related to the following three products: AK Forte; Infla-650 and Umary.
Tags: Pharma, Adverse Event, 2024
Tags: Pharma, Adverse Event, 2024
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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