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FDA Toxicity Study Reports on Fucoxanthin (NDIN 1048)
FDA Toxicity Study Reports on Fucoxanthin (NDIN 1048)
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Original Request: As permitted by the Freedom of Information Act (FOIA), I am hereby requesting the following document(s) in electronic PDF: • All study reports and supporting data pertaining to all toxicity studies conducted using Fucoxanthin, as described in the NDIN 1048, submitted by Algatechnologies.
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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