# FDA Inspection 1033906 - GERI-GENTLE CORPORATION - December 04, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/geri-gentle-corporation/9151ad5b-ecf3-45ba-b588-75aa4ac504e1
Source feed: FDA_Inspections

> FDA Inspection 1033906 for GERI-GENTLE CORPORATION on December 04, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1033906
- Company Name: GERI-GENTLE CORPORATION
- Inspection Date: 2017-12-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1033906 - 2017-12-04](https://www.globalkeysolutions.net/records/fda_inspections/geri-gentle-corporation/8209fa02-a4cb-4a05-bd1b-c63eaa45d449)

Company: https://www.globalkeysolutions.net/companies/geri-gentle-corporation/2d4c3127-645d-4f1b-bf67-a10b8ea209c1

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