Interpore Cross International, LLC

Form 483

Irvine, California, United StatesFEI 1000160576Issued January 23, 2013

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1000160576.

Observations2

Issue DateJanuary 23, 2013

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Interpore Cross International, LLC
Location: Irvine, California, United States
FEI Number: 1000160576
Product Type: Devices
Issue Date: January 23, 2013
Country: United States

Inspection History, 2013 to 2025

NAI3

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Interpore Cross International, LLC FDA Form 483, Irvine, California, January 23, 2013