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Neoss Ab 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 3008517673.

Neoss Ab

Molnlycke, -, Sweden
Issue DateSeptember 22, 2010
FEI Number3008517673
CountrySweden
Status
No Warning Letter
Product Type
Devices
Neoss Ab FDA Form 483, Molnlycke, September 22, 2010