FDA Inspection
Medron, LLCMedron, LLC – FDA Inspection, Nov 1, 2013
Record Details
This FDA Inspection record concerns Medron, LLC, with an inspection on November 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medron, LLC
- Inspection Date
- November 1, 2013
- Product Type
- Devices
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ID · f35aa353-63a7-4929-a4c3-e2e40b5cb3f4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 861058
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medron, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 20, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 12, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 3, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 21, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Medron, LLC
- FDA Inspection 1333920 - 2026-08-20
- FDA Inspection 1114073 - 2019-12-12
- FDA Inspection 893698 - 2014-09-03
- FDA Inspection 720950 - 2011-04-21
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