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•United States

Defibtech, LLC, Guilford, CT – FDA Inspections

Inspection records and compliance data for Defibtech, LLC in Guilford, Connecticut. 5 FDA inspections on record (1 OAI), last inspected August 16, 2017.

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Company Profile

This profile covers Defibtech, LLC based in Guilford, Connecticut, United States.

FDA Inspection History

FDA inspections
5
OAI
1
VAI
1
NAI
3
Form 483s
0
Warning letters
0

First inspected August 18, 2010. Last inspected August 16, 2017.

Most cited issue areas

  • Nonconforming product, Lack of or inadequate procedures1 inspection

FDA inspections (5)

DateResultFDA center(s)Insp. #
August 16, 2017NAIMedical Devices & Rad Health · Compliance: Devices1024269
April 25, 2014NAIMedical Devices & Rad Health · Compliance: Devices876495
December 21, 2011NAIMedical Devices & Rad Health · Compliance: Devices760057
February 8, 2011VAIMedical Devices & Rad Health · Compliance: Devices708589
August 18, 2010OAIMedical Devices & Rad Health · Compliance: Devices675878
FDA documents

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

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Northeast Scientific Inc.
Light Sources, Inc.
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AGP-Medical, LLC
Z-Medica, LLC
Northeast Resins & Silicones, LLC
Company Information

Name

Defibtech, LLC

FEI Number

3003521780

Address

741 Boston Post Rd Ste 201, Guilford, Connecticut 06437, United States

Country

United States

ID: 2d1df48a-49ee-431d-8535-840d912c1f36

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