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 3000719482.
Observations1
Issue DateFebruary 26, 2013
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Endoplus
Location
Mundelein, Illinois, United States
FEI Number
3000719482
Product Type
Devices
Issue Date
February 26, 2013
Country
United States
Inspection History, 2009 to 2026
NAI4
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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