FDA Inspection
Okido Ltd.Okido Ltd. – FDA Inspection, Jun 4, 2010
Record Details
This FDA Inspection record concerns Okido Ltd., with an inspection on June 4, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Okido Ltd.
- Inspection Date
- June 4, 2010
- Product Type
- Devices
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ID · a8dfdc13-1d7a-44a1-93e9-c9df2793a8c1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 665195
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Okido Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 30, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 17, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Okido Ltd.
- FDA Inspection 864357 - 2014-01-30
- FDA Inspection 768169 - 2012-02-17
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