# FDA Inspection 1066052 - Alan Neuromedical Technologies - September 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/alan-neuromedical-technologies/9e57ab8a-5783-433c-a40e-28cc49face0e
Source feed: FDA_Inspections

> FDA Inspection 1066052 for Alan Neuromedical Technologies on September 13, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066052
- Company Name: Alan Neuromedical Technologies
- Inspection Date: 2018-09-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1066052 - 2018-09-13](https://www.globalkeysolutions.net/records/fda_inspections/alan-neuromedical-technologies/888a9c39-6158-4d16-93fc-e8d41499ca0d)
- [FDA Inspection 904809 - 2014-11-05](https://www.globalkeysolutions.net/records/fda_inspections/alan-neuromedical-technologies/35a14c46-77e6-41b6-8621-ab96765f5b20)
- [FDA Inspection 721842 - 2011-04-08](https://www.globalkeysolutions.net/records/fda_inspections/alan-neuromedical-technologies/6e6d0a80-0a72-48b4-903a-9237e52c2c40)

Company: https://www.globalkeysolutions.net/companies/alan-neuromedical-technologies/35919b37-7b42-411c-84e3-66b9eeb4a70c

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