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 3004717358.
Observations2
Issue DateMarch 22, 2024
StatusNo Warning Letter
Related Inspections5
Establishment Details
Firm
SpineCraft, LLC.
Location
Westmont, Illinois, United States
FEI Number
3004717358
Product Type
Devices
Issue Date
March 22, 2024
Country
United States
Inspection History, 2012 to 2024
NAI4
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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