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Kenji Ando, M.D. 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.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 1000585154.

Kenji Ando, M.D.

Kitakyushu, -, Japan
Issue DateJuly 17, 2014
FEI Number1000585154
CountryJapan
Status
No Warning Letter
Product Type
Devices
Kenji Ando, M.D. FDA Form 483, Kitakyushu, July 17, 2014