# GERI-GENTLE CORPORATION – FDA Inspection, Dec 4, 2017

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

> FDA inspection 1033906 of GERI-GENTLE CORPORATION, December 04, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

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

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