# FDA Inspection 1171545 - NEURELEC - June 02, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/neurelec/68e51f96-aab2-453a-8769-614e9295aa6d
Source feed: FDA_Inspections

> FDA Inspection 1171545 for NEURELEC on June 02, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1171545
- Company Name: NEURELEC
- Inspection Date: 2022-06-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1171545 - 2022-06-02](https://www.globalkeysolutions.net/records/fda_inspections/neurelec/9c0c9a8c-bf75-44a8-b545-4ffcdb58b308)

Company: https://www.globalkeysolutions.net/companies/neurelec/7e121ac2-8de5-4034-b39b-f4768d711b5d

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