FDA Inspection
Verticor, LtdVerticor, Ltd – FDA Inspection, Aug 5, 2010
Record Details
This FDA Inspection record concerns Verticor, Ltd, with an inspection on August 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Verticor, Ltd
- Inspection Date
- August 5, 2010
- Product Type
- Devices
View Company Profile
ID · a5229dd8-d24c-46b3-aea0-7776ff84bbf0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 676597
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.198(a)Complaints
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.22Quality Audits - defined intervals
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