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FDA Inspection
•Lucas Medical, Inc.•February 24, 2009

Lucas Medical, Inc. – FDA Inspection, Feb 24, 2009

Record Details

This FDA Inspection record concerns Lucas Medical, Inc., with an inspection on February 24, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Lucas Medical, Inc.
Inspection Date
February 24, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 4e7c4da8-58d8-4a96-85dc-b7c0ae70ae3b

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
567177
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

3
  1. 21 CFR 820.198(a)General
  2. 21 CFR 820.198(c)Investigation of device failures
  3. 21 CFR 820.100(b)Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Lucas Medical, Inc.

3
DateClassificationOfficeProject area
July 15, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
May 24, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
November 24, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Lucas Medical, Inc.
  • FDA Inspection 1245519 - 2024-07-15
  • FDA Inspection 1054303 - 2018-05-24
  • FDA Inspection 907290 - 2014-11-24

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