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•United States

Nuvolase Inc., Los Angeles, CA – FDA Inspections

Inspection records and compliance data for Nuvolase Inc. in Los Angeles, California. 4 FDA inspections on record (1 OAI), 1 Form 483, 1 warning letter, last inspected May 23, 2018.

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Company Profile

This profile covers Nuvolase Inc. based in Los Angeles, California, United States.

FDA Inspection History

FDA inspections
4
OAI
1
VAI
1
NAI
2
Form 483s
1
Warning letters
1

First inspected May 3, 2010. Last inspected May 23, 2018.

Most cited issue areas

  • Approval, inadequate purchasing data1 inspection
  • Design verification - output does not meet input requirement1 inspection
  • Failure to report1 inspection

FDA inspections (4)

DateResultFDA center(s)Insp. #
May 23, 2018VAIMedical Devices & Rad Health · Radiation Control and Health Safety Act1052985
March 13, 2015NAIMedical Devices & Rad Health · Postmarket Assurance: Devices917181
September 20, 2013OAIMedical Devices & Rad Health · Compliance: Devices850450
May 3, 2010NAIMedical Devices & Rad Health · Postmarket Assurance: Devices652943
FDA documents

Warning Letters (1)

  • Warning Letters · September 20, 2013
People (1)
Kathleen M. Lewis
Person
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Company Information

Name

Nuvolase Inc.

FEI Number

3007590700

Address

10921 Wilshire Blvd Ste 1011, Los Angeles, California 90024, United States

Country

United States

ID: ce2cec64-0104-45aa-9ac4-98aefe7e3e1f

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