FDA Inspection
LDR MedicalLDR Medical – FDA Inspection, Jul 9, 2009
Record Details
This FDA Inspection record concerns LDR Medical, with an inspection on July 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LDR Medical
- Inspection Date
- July 9, 2009
- Product Type
- Devices
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ID · c79798fb-9deb-4f11-b6ed-d584b9defd5d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 600305
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.80(b)Incoming inspection, testing, verification
- 21 CFR 820.181(c)DMR QA procedures and specifications
- 21 CFR 820.181(d)DMR packaging and labeling specifications
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Other FDA inspections of LDR Medical
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 7, 2025 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 4, 2014 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for LDR Medical
- FDA Inspection 1266093 - 2025-04-07
- FDA Inspection 905792 - 2014-12-04
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