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 1000123280.
Observations2
Issue DateNovember 04, 2011
StatusNo Warning Letter
Related Inspections3
Establishment Details
Firm
Kerma Medical Products, Inc
Location
Suffolk, Virginia, United States
FEI Number
1000123280
Product Type
Devices
Issue Date
November 04, 2011
Country
United States
Inspection History, 2011 to 2017
NAI1
VAI2
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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