FDA Inspection
Lone Star Medical Products, Inc.Lone Star Medical Products, Inc. – FDA Inspection, Sep 23, 2014
Record Details
This FDA Inspection record concerns Lone Star Medical Products, Inc., with an inspection on September 23, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 23, 2014
- Product Type
- Devices
View Company Profile
ID · ecffea06-5659-420b-9806-bc8d895b8ddf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896250
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: 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 |
| May 4, 2017 | NAI | Center for Devices and Radiological Health | Compliance: 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 1021325 - 2017-05-04
- FDA Inspection 793298 - 2012-08-06
- FDA Inspection 711363 - 2011-02-24
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