483
Overjet, Inc.Overjet, Inc. – FDA 483
Record Details
This FDA Form 483 was issued to Overjet, Inc. No specific inspectional observations or findings are detailed in the provided document. The report appears to be a minimal record release related to a change request.
- Company
- Overjet, Inc.
- Product type
- device
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ID · 1f04235d-de6a-47ab-8983-5b21eec908c4
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