# Medtimo Inc – FDA Inspection, Feb 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/medtimo-inc/ea213f74-220c-4cd4-8d18-2e82ebe73e8d
Source feed: FDA_Inspections

> FDA inspection 1041724 of Medtimo Inc, February 15, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1041724
- Company Name: Medtimo Inc
- Inspection Date: 2018-02-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1035426 - 2017-11-13
- FDA Inspection 993558 - 2016-11-03
- [FDA Inspection 968712 - 2016-05-04](https://www.keypedia.com/records/fda_inspections/medtimo-inc/6036f5c4-a2f9-4202-ae8b-ab3c72271d6d)
- FDA Inspection 912086 - 2015-01-23
- [FDA Inspection 884334 - 2014-06-18](https://www.keypedia.com/records/fda_inspections/medtimo-inc/113a9060-f3b8-4861-90a8-cc5fd58ddf83)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sonya-l-karsik/c24603b9-5ca0-46f5-861a-b367155b0def)

Company: https://www.keypedia.com/companies/medtimo-inc/f476822e-d110-4a3f-9ab4-db3ec11231f3

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