# FDA Inspection 1043580 - Vidatak LLC - February 02, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/vidatak-llc/fa4f0db0-a2b5-4977-b239-9e2bbc757324/
Source feed: FDA_Inspections

> FDA Inspection 1043580 for Vidatak LLC on February 02, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1043580
- Company Name: Vidatak LLC
- Inspection Date: 2018-02-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1043580 - 2018-02-02](https://www.globalkeysolutions.net/api/records/fda_inspections/vidatak-llc/1b89354e-4b65-4a55-8364-82edab2e344d/)
- [FDA Inspection 939944 - 2015-08-27](https://www.globalkeysolutions.net/api/records/fda_inspections/vidatak-llc/39f57fb1-294a-4938-b53b-cfce93f42335/)
- [FDA Inspection 939944 - 2015-08-27](https://www.globalkeysolutions.net/api/records/fda_inspections/vidatak-llc/1b67284d-a953-4934-a919-d9bb2ea4105a/)

Company: https://www.globalkeysolutions.net/companies/vidatak-llc/3836158f-580d-4480-9379-1539272b187e

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