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•United States

Kerma Medical Products, Inc, Suffolk, VA – FDA Inspections

Inspection records and compliance data for Kerma Medical Products, Inc in Suffolk, Virginia. 3 FDA inspections on record, last inspected July 07, 2017.

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Company Profile

This profile covers Kerma Medical Products, Inc based in Suffolk, Virginia, United States.

FDA Inspection History

FDA inspections
3
OAI
0
VAI
2
NAI
1
Form 483s
0
Warning letters
0

First inspected November 4, 2011. Last inspected July 7, 2017.

Most cited issue areas

  • Design transfer - Lack of or inadequate procedures1 inspection
  • Design validation- Lack of or inadequate procedures1 inspection
  • Design verification - Lack of or inadequate procedures1 inspection

FDA inspections (3)

DateResultFDA center(s)Insp. #
July 7, 2017NAIMedical Devices & Rad Health · Postmarket Assurance: Devices1024609
January 23, 2014VAIMedical Devices & Rad Health · Compliance: Devices863395
November 4, 2011VAIMedical Devices & Rad Health · Compliance: Devices752181
FDA documents

No Form 483s, Warning Letters or EIRs on record.

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Company Information

Name

Kerma Medical Products, Inc

FEI Number

1000123280

Address

215 Suburban Dr, Suffolk, Virginia 23434, United States

Country

United States

ID: bb96e435-46df-43ce-b968-771b7abe04f3

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