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Anodyne Surgical 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 1929756.

Anodyne Surgical

Saint Charles, Missouri, United States
Issue DateApril 25, 2018
FEI Number1929756
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Anodyne Surgical FDA Form 483, Saint Charles, Missouri, April 25, 2018