# LED Technologies, LLC, Greenwood Village, CO – FDA Inspections

Source: https://www.keypedia.com/companies/led-technologies-llc/c72c5291-7d40-44a0-af61-098a8437af67

> Inspection records and compliance data for LED Technologies, LLC in Greenwood Village, Colorado. 4 FDA inspections on record, 1 Form 483, last inspected April 12, 2018.

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## Details

- Name: LED Technologies, LLC
- FEI Number: 3006315288
- Address Line 1: 6000 Greenwood Plaza Blvd Ste 110
- City: Greenwood Village
- State: Colorado
- Zip Code: 80111
- Country Name: United States
- Address: 6000 Greenwood Plaza Blvd Ste 110, Greenwood Village, Colorado 80111, United States
- Country: United States

## Related Documents

- [FDA Inspection 1048041 - LED Technologies, LLC - 2018-04-12](https://www.keypedia.com/records/fda_inspections/led-technologies-llc/a50c1dc1-219e-466b-9a65-6990291619ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2018
- FDA Inspection 1048041 - LED Technologies, LLC - 2018-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2018
- FDA Inspection 981430 - LED Technologies, LLC - 2016-06-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2016
- FDA Inspection 981430 - LED Technologies, LLC - 2016-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2016
- FDA Inspection 800774 - LED Technologies, LLC - 2012-09-25 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2012
- [FDA Inspection 800774 - LED Technologies, LLC - 2012-09-25](https://www.keypedia.com/records/fda_inspections/led-technologies-llc/71428b0c-c1b1-4170-ab72-07ce52214875) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 25, 2012
- FDA Inspection 579085 - LED Technologies, LLC - 2009-04-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 22, 2009
- FDA Inspection 579085 - LED Technologies, LLC - 2009-04-22 — classification: No Action Indicated (NAI), source: FDA, date: April 22, 2009

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