FDA Inspection
Aspide MedicalAspide Medical – FDA Inspection, Sep 27, 2012
Record Details
This FDA Inspection record concerns Aspide Medical, with an inspection on September 27, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Aspide Medical
- Inspection Date
- September 27, 2012
- Product Type
- Devices
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ID · b46590c3-24f1-409d-b2bb-ad625d2a822f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 803735
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.200(c)Service reports/MDRs/complaints
- 21 CFR 820.40(a)Document review, approval documentation
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Other FDA inspections of Aspide Medical
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 23, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Aspide Medical
- FDA Inspection 937908 - 2015-07-23
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