# FDA Inspection 1041913 - eNeura, Inc. - January 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/eneura-inc/b6e0614f-e539-4963-85bb-e6611b531cea
Source feed: FDA_Inspections

> FDA Inspection 1041913 for eNeura, Inc. on January 11, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1041913
- Company Name: eNeura, Inc.
- Inspection Date: 2018-01-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1041913 - 2018-01-11](https://www.keypedia.com/records/fda_inspections/eneura-inc/920dbba2-3b64-4eb0-aee0-3951829e9e67)

Company: https://www.keypedia.com/companies/eneura-inc/132188ae-a392-402f-b375-84183d02af7e

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