# FDA Inspection 1054737 - Refocus Group, Inc. - May 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/refocus-group-inc/97c6d348-0243-4993-8031-5b7a97223273
Source feed: FDA_Inspections

> FDA Inspection 1054737 for Refocus Group, Inc. on May 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054737
- Company Name: Refocus Group, Inc.
- Inspection Date: 2018-05-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055655 - 2018-05-24](https://www.globalkeysolutions.net/records/fda_inspections/refocus-group-inc/e06ea0fa-3ca9-4506-803b-005c4b645bd2)
- [FDA Inspection 649211 - 2010-03-10](https://www.globalkeysolutions.net/records/fda_inspections/refocus-group-inc/dd467286-73d1-4c4f-8e77-ac49d11aba15)

Company: https://www.globalkeysolutions.net/companies/refocus-group-inc/75145ac6-4c80-4894-b742-814e421a9f88

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