# VIDAR Systems Corp, Herndon, VA – FDA Inspections

Source: https://www.keypedia.com/companies/vidar-systems-corp/7f36c416-8a1b-4560-b381-63df50e0307f

> Inspection records and compliance data for VIDAR Systems Corp in Herndon, Virginia. 5 FDA inspections on record, last inspected October 08, 2021.

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## Details

- Name: VIDAR Systems Corp
- FEI Number: 2027116
- Address Line 1: 365 Herndon Pkwy Ste 105
- City: Herndon
- State: Virginia
- Zip Code: 20170
- Country Name: United States
- Address: 365 Herndon Pkwy Ste 105, Herndon, Virginia 20170, United States
- Country: United States

## Related Documents

- FDA Inspection 1155929 - VIDAR Systems Corp - 2021-10-08 — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2021
- [FDA Inspection 1155929 - VIDAR Systems Corp - 2021-10-08](https://www.keypedia.com/records/fda_inspections/vidar-systems-corp/a261e23e-7b62-4d15-8d1d-406b0eeffb9d) — classification: No Action Indicated (NAI), source: FDA, date: October 8, 2021
- FDA Inspection 1068361 - VIDAR Systems Corp - 2018-09-21 — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2018
- FDA Inspection 930039 - VIDAR Systems Corp - 2015-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2015
- FDA Inspection 930039 - VIDAR Systems Corp - 2015-06-11 — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2015
- [FDA Inspection 798394 - VIDAR Systems Corp - 2012-08-29](https://www.keypedia.com/records/fda_inspections/vidar-systems-corp/a16c1c65-bc64-4e9d-8a04-e3811e5257f3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 29, 2012
- FDA Inspection 798394 - VIDAR Systems Corp - 2012-08-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 29, 2012
- FDA Inspection 735684 - VIDAR Systems Corp - 2011-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2011
- FDA Inspection 735684 - VIDAR Systems Corp - 2011-07-21 — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2011

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