FDA Inspection
Technology Delivery Systems IncTechnology Delivery Systems Inc – FDA Inspection, May 11, 2011
Record Details
This FDA Inspection record concerns Technology Delivery Systems Inc, with an inspection on May 11, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 11, 2011
- Product Type
- Devices
View Company Profile
ID · a2f1ddb2-9524-4271-a7be-9a22c0f87be1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 724548
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
8- 21 CFR 820.75(c)Process changes - review, evaluation and revalidation
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.198(e)Records of complaint investigation
- 21 CFR 820.184DHR content
- 21 CFR 820.50(b)Supplier notification of changes
Full citation text and observation details available on the Dashboard.
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 |
| March 24, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Technology Delivery Systems Inc
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.