FDA Inspection
DIO USADIO USA – FDA Inspection, May 12, 2010
Record Details
This FDA Inspection record concerns DIO USA, with an inspection on May 12, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DIO USA
- Inspection Date
- May 12, 2010
- Product Type
- Devices
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ID · e9cd46c7-a113-4761-b3e3-9fba938695d9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 661058
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.18(d)(1)Distributor responsibilities for complaint records
Full citation text and observation details available on the Dashboard.
Other FDA inspections of DIO USA
1| Date | Classification | Office | Project area |
|---|---|---|---|
| November 16, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for DIO USA
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