# FDA Inspection 606798 - ELITechGroup, Inc. - July 01, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/420488fb-5cb0-400b-acae-392b626dc552
Source feed: FDA_Inspections

> FDA Inspection 606798 for ELITechGroup, Inc. on July 01, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 606798
- Company Name: ELITechGroup, Inc.
- Inspection Date: 2009-07-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1021632 - 2017-08-11](https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/dcfe5642-67db-4c25-8b1f-558a86553ebe)
- [FDA Inspection 1021632 - 2017-08-11](https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/d785dce2-6639-4671-95c7-98eaefed6a6e)
- [FDA Inspection 930474 - 2015-05-27](https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/f19fc836-e90c-482a-9fa3-2388e45303f8)
- [FDA Inspection 930474 - 2015-05-27](https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/df56699d-9400-44e3-bbf8-236eb8f00d99)
- [FDA Inspection 737028 - 2011-07-22](https://www.globalkeysolutions.net/records/fda_inspections/elitechgroup-inc/cd0f7a3c-7bbc-4652-b8d6-acb36fec2c24)

Company: https://www.globalkeysolutions.net/companies/elitechgroup-inc/1b1d6fc5-1f06-40f4-ba42-c2d59ed468d4

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7