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FDA Form 483 for Keranetics Inc. Inspection Ending Feb 6, 2025 – Devices Compliance
FDA Form 483 for Keranetics Inc. Inspection Ending Feb 6, 2025 – Devices Compliance
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Original Request: To Whom it May Concern: As permitted by the Freedom of Information Act (FOIA), I am hereby requesting the following document: Form FDA 483: Keranetics Inc. Winston Salem, North Carolina United States End Dates of inspection: 06 Feb 2025 Project Area: Compliance: Devices FEI: 3015980493 Classification: VAI
Tags: MedTech, 483, 2025
Tags: MedTech, 483, 2025
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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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