FDA Inspection
Technology Delivery Systems IncTechnology Delivery Systems Inc – FDA Inspection, Mar 24, 2009
Record Details
This FDA Inspection record concerns Technology Delivery Systems Inc, with an inspection on March 24, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 24, 2009
- Product Type
- Devices
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ID · 416ba22a-cd2c-4169-a67a-5683bf57e012
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 570375
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.100(b)Documentation
- 21 CFR 820.20(c)Management review - Lack of or inadequate procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.22Quality Audit/Reaudit - documentation
- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of Technology Delivery Systems Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 15, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 25, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 11, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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