FDA Inspection
Nissha Medical Technologies (Ohio), Inc.Nissha Medical Technologies (Ohio), Inc. – FDA Inspection, Oct 28, 2011
Record Details
This FDA Inspection record concerns Nissha Medical Technologies (Ohio), Inc., with an inspection on October 28, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 28, 2011
- Product Type
- Devices
View Company Profile
ID · 68ec7896-6289-4481-8a10-daa21e106642
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 752679
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
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Other FDA inspections of Nissha Medical Technologies (Ohio), Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 15, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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