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Harps Europe Manufacturing 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 3007478974.

Harps Europe Manufacturing

Wimpassing Im Schwarzatale, -, Austria
Issue DateMay 28, 2010
FEI Number3007478974
CountryAustria
Status
No Warning Letter
Product Type
Devices
Harps Europe Manufacturing FDA Form 483, Wimpassing Im Schwarzatale, May 28, 2010