FDA Inspection
Barton-Carey Medical Products IncBarton-Carey Medical Products Inc – FDA Inspection, Sep 4, 2009
Record Details
This FDA Inspection record concerns Barton-Carey Medical Products Inc, with an inspection on September 4, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 4, 2009
- Product Type
- Devices
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ID · 38de609c-a5cd-4a0a-9f2d-a5385c18c62d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 612341
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.198(a)General
- 21 CFR 820.80(d)(3)No release signature
- 21 CFR 820.80(d)(4)No release authorization date
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Barton-Carey Medical Products Inc
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 14, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 10, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
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