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 3005584379.
Observations2
Issue DateJuly 29, 2011
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
Neumann's Home Medical Equipment, Inc.
Location
Aurora, Illinois, United States
FEI Number
3005584379
Product Type
Drugs
Issue Date
July 29, 2011
Country
United States
Inspection History, 2011 to 2014
NAI1
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.