FDA Inspection
Smisson-Cartledge Biomedical, LLCSmisson-Cartledge Biomedical, LLC – FDA Inspection, May 16, 2014
Record Details
This FDA Inspection record concerns Smisson-Cartledge Biomedical, LLC, with an inspection on May 16, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 16, 2014
- Product Type
- Devices
View Company Profile
ID · 22e32056-307c-4a6b-9e31-6f1b4fadac2b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 881133
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.40Procedures not adequately established or maintained
- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Smisson-Cartledge Biomedical, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 28, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 15, 2011 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 18, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Smisson-Cartledge Biomedical, LLC
- FDA Inspection 1220867 - 2023-09-15
- FDA Inspection 1047469 - 2018-02-28
- FDA Inspection 754932 - 2011-11-15
- FDA Inspection 619266 - 2009-09-18
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