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Avalign Delivery Systems Division 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 3000717687.

Avalign Delivery Systems Division

Greenwood, Indiana, United States
Issue DateMay 23, 2018
FEI Number3000717687
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Avalign Delivery Systems Division FDA Form 483, Greenwood, Indiana, May 23, 2018