483
ABK Biomedical IncABK Biomedical Inc – FDA 483
Record Details
This document, intended as an FDA Form 483 inspectional-observation report for ABK Biomedical Inc, contains no specific observations. The provided context appears to be an email exchange related to an FDA submission (K220567/S001) and a FOIA request, rather than an inspection report.
- Company
- ABK Biomedical Inc
- Product type
- device
- Office
- Human Foods Program
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ID · 63ef81ae-1d07-4fa3-a788-80ed68c0b1c1
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