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•United States

Kenlor Industries, Inc., Santa Ana, CA – FDA Inspections

Inspection records and compliance data for Kenlor Industries, Inc. in Santa Ana, California. 3 FDA inspections on record (1 OAI), 2 Form 483s, last inspected September 21, 2020.

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Company Profile

This profile covers Kenlor Industries, Inc. based in Santa Ana, California, United States.

FDA Inspection History

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

First inspected June 2, 2017. Last inspected September 21, 2020.

Most cited issue areas

  • Calibration, Inspection, etc. Procedures Lack of or Inadequ2 inspections
  • Design control - no procedures1 inspection
  • DMR - not or inadequately maintained1 inspection

FDA inspections (3)

DateResultFDA center(s)Insp. #
September 21, 2020VAIMedical Devices & Rad Health · Compliance: Devices1129642
May 3, 2019OAIMedical Devices & Rad Health · Compliance: Devices1088389
June 2, 2017Not classifiedMedical Devices & Rad Health1021555
FDA documents

Form 483s (2)

  • Form 483s · September 21, 2020
  • Form 483s · May 3, 2019
People (2)
Janet Pulver
Person
Creighton T. Tuzon
Person
Related Companies (10)

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ULab Systems, Inc.
Cerus Corporation
MONOCENT INC.
Company Information

Name

Kenlor Industries, Inc.

FEI Number

2027370

Address

1560 E Edinger Ave Ste A1, Santa Ana, California 92705, United States

Country

United States

ID: cd8019cb-691d-4735-9728-add884b0aead

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