FDA Inspection
Morris Innovative, Inc.Morris Innovative, Inc. – FDA Inspection, Feb 1, 2013
Record Details
This FDA Inspection record concerns Morris Innovative, Inc., with an inspection on February 1, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Morris Innovative, Inc.
- Inspection Date
- February 1, 2013
- Product Type
- Devices
View Company Profile
ID · 6419ce27-7e01-453a-958c-8da7a2d65f18
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819336
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(b)Documentation
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Morris Innovative, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 22, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 22, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Morris Innovative, Inc.
- FDA Inspection 958725 - 2016-01-26
- FDA Inspection 700412 - 2010-10-22
- FDA Inspection 697076 - 2010-10-22
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