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Interpore Cross International, LLC 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 1000160576.

Interpore Cross International, LLC

Irvine, California, United States
Issue DateJanuary 23, 2013
FEI Number1000160576
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Interpore Cross International, LLC FDA Form 483, Irvine, California, January 23, 2013