FDA Inspection
Lone Star Medical Products, Inc.Lone Star Medical Products, Inc. – FDA Inspection, May 4, 2017
Record Details
This FDA Inspection record concerns Lone Star Medical Products, Inc., with an inspection on May 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6f8e44ba-6ec9-4328-bfe4-99c2a48245d2
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1021325
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Lone Star Medical Products, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 27, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 2, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 23, 2014 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 6, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 24, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Lone Star Medical Products, Inc.
- FDA Inspection 1203824 - 2023-04-27
- FDA Inspection 1057460 - 2018-05-02
- FDA Inspection 896250 - 2014-09-23
- FDA Inspection 793298 - 2012-08-06
- FDA Inspection 711363 - 2011-02-24
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