# Technology Delivery Systems Inc, New Orleans, LA – FDA Inspections

Source: https://www.keypedia.com/companies/technology-delivery-systems-inc/ec509742-b990-4320-b479-209a7d22c202

> Inspection records and compliance data for Technology Delivery Systems Inc in New Orleans, Louisiana. 4 FDA inspections on record, last inspected March 15, 2016.

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## Details

- Name: Technology Delivery Systems Inc
- FEI Number: 3004088999
- Address Line 1: 512 Verret St
- City: New Orleans
- State: Louisiana
- Zip Code: 70114
- Country Name: United States
- Address: 512 Verret St, New Orleans, Louisiana 70114, United States
- Country: United States

## Related Documents

- [FDA Inspection 983494 - Technology Delivery Systems Inc - 2016-03-15](https://www.keypedia.com/records/fda_inspections/technology-delivery-systems-inc/37704250-4ff7-4f5d-9300-e4c40370e207) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 15, 2016
- [FDA Inspection 841079 - Technology Delivery Systems Inc - 2013-06-25](https://www.keypedia.com/records/fda_inspections/technology-delivery-systems-inc/b2be92c8-b43c-40f6-ab98-df7953456ebc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 25, 2013
- [FDA Inspection 724548 - Technology Delivery Systems Inc - 2011-05-11](https://www.keypedia.com/records/fda_inspections/technology-delivery-systems-inc/a2f1ddb2-9524-4271-a7be-9a22c0f87be1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2011
- FDA Inspection 724548 - Technology Delivery Systems Inc - 2011-05-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 11, 2011
- [FDA Inspection 570375 - Technology Delivery Systems Inc - 2009-03-24](https://www.keypedia.com/records/fda_inspections/technology-delivery-systems-inc/416ba22a-cd2c-4169-a67a-5683bf57e012) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2009
- FDA Inspection 570375 - Technology Delivery Systems Inc - 2009-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2009

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