# FDA Inspection 939944 - Vidatak LLC - August 27, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/vidatak-llc/39f57fb1-294a-4938-b53b-cfce93f42335
Source feed: FDA_Inspections

> FDA Inspection 939944 for Vidatak LLC on August 27, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 939944
- Company Name: Vidatak LLC
- Inspection Date: 2015-08-27
- 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/records/fda_inspections/vidatak-llc/fa4f0db0-a2b5-4977-b239-9e2bbc757324)
- [FDA Inspection 1043580 - 2018-02-02](https://www.globalkeysolutions.net/records/fda_inspections/vidatak-llc/1b89354e-4b65-4a55-8364-82edab2e344d)
- [FDA Inspection 939944 - 2015-08-27](https://www.globalkeysolutions.net/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
