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Buxton Biomedical Inc Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

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Buxton Biomedical Inc

East Hanover, New Jersey, United States
Issue DateJuly 27, 2009
FEI Number1000208866
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Buxton Biomedical Inc FDA Form 483, East Hanover, New Jersey, July 27, 2009