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 2023050.
Observations6
Issue DateJanuary 29, 2009
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Newport Medical Instruments Inc
Location
Costa Mesa, California, United States
FEI Number
2023050
Product Type
Devices
Issue Date
January 29, 2009
Country
United States
Inspection History, 2009 to 2017
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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