# GTIMD LLC – FDA Inspection, Oct 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/gtimd-llc/903dbb14-9170-4220-b2be-bfc6ad6af779
Source feed: FDA_Inspections

> FDA inspection 1069209 of GTIMD LLC, October 17, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069209
- Company Name: GTIMD LLC
- Inspection Date: 2018-10-17
- 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: 1

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/gtimd-llc/fb71f836-8a97-4ee5-87a5-4ed1e73071ba

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