FDA Inspection
D.M. Davis IncorporatedD.M. Davis Incorporated – FDA Inspection, Jun 9, 2009
Record Details
This FDA Inspection record concerns D.M. Davis Incorporated, with an inspection on June 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- D.M. Davis Incorporated
- Inspection Date
- June 9, 2009
- Product Type
- Devices
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ID · c794ef90-2056-48f4-b7d3-e43dd3a7c96c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 586870
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
6- 21 CFR 820.80(b)Incoming acceptance records, documentation
- 21 CFR 820.100(a)(1)Procedure for analysis of data sources
- 21 CFR 820.184DHR content
- 21 CFR 820.181(a)DMR device specifications
- 21 CFR 820.72(b)(2)Calibration documentation
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of D.M. Davis Incorporated
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 19, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for D.M. Davis Incorporated
- FDA Inspection 790775 - 2012-07-19
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