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FDA Form 483s for Vivos Therapeutics, Chemsil, ALOM Tech, Exactech, and Nihon Kohden – Devices
FDA Form 483s for Vivos Therapeutics, Chemsil, ALOM Tech, Exactech, and Nihon Kohden – Devices
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Original Request: Please provide the following inspection-related document(s) in electronic PDF format related to Devices product type: The 483(s) (in electronic format) for the inspection of Vivos Therapeutics Inc. (FEI 3022315836), located in Murray, Kentucky, United States, inspection ending 2024-10-24. The 483(s) (in electronic format) for the inspection of Chemsil Silicones Inc (FEI 3009939047), located in Chatsworth, California, United States, inspection ending 2024-10-22. The 483(s) (in electronic format) for the inspection of ALOM Technologies Corporation (FEI 3015489159), located in Indianapolis, Indiana, United States, inspection ending 2024-10-17. The 483(s) (in electronic format) for the inspection of Exactech, Inc. (FEI 1038671), located in Gainesville, Florida, United States, inspection ending 2024-10-09. The 483(s) (in electronic format) for the inspection of Nihon Kohden America LLC (FEI 2080783), located in Irvine, California, United States, inspection ending 2024-10-04.
Tags: MedTech, 483, 2024
Tags: MedTech, 483, 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. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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