483
Remington Medical, Inc.FDA 483 - Remington Medical, Inc.
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Record Details
This FDA Form 483 inspection report for Remington Medical, Inc. indicates that no inspectional observations were cited during the inspection. The document primarily consists of administrative information related to a FOIA request.
- Company
- Remington Medical, Inc.
- Product Type
- Device
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ID · 5276aee9-0d33-41b3-bd57-6586f0be6a19