FDA Inspection
Towic Medical Inc.Towic Medical Inc. – FDA Inspection, Sep 9, 2011
Record Details
This FDA Inspection record concerns Towic Medical Inc., with an inspection on September 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Towic Medical Inc.
- Inspection Date
- September 9, 2011
- Product Type
- Devices
View Company Profile
ID · 73c1bdbe-406c-42a3-bd7e-67e1ea0eb930
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 743924
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
- 21 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
- 21 CFR 820.120Lack of or inadequate procedures for labeling
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Towic Medical Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 3, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Towic Medical Inc.
- FDA Inspection 872901 - 2014-04-03
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