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FDA Dynarex Baby Powder Testing and Recall – Correspondence and Meeting Records
FDA Dynarex Baby Powder Testing and Recall – Correspondence and Meeting Records
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Original Request: Any correspondence, meeting minutes, or memoranda between the FDA and any third parties, including but not limited to the testing laboratory, related to the testing, recall decision, and FDA’s announcement regarding Dynarex Corporation’s Dynacare Baby Powder, item number 4875, Batch Number B 051, which is available at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dynarex-corporation-recalls-product-due-possible-health-risk#:~:text=Montvale%2C%20NJ%2C%20September%2019%2C,ingredient%20in%20many%20cosmetic%20products
Tags: Pharma, Recall, 2019
Tags: Pharma, Recall, 2019
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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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