# FDA Inspection 823160 - Neuropace Inc - March 05, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/neuropace-inc/f7cd7549-8bd5-4eee-adab-3db41d2ea5f6/
Source feed: FDA_Inspections

> FDA Inspection 823160 for Neuropace Inc on March 05, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823160
- Company Name: Neuropace Inc
- Inspection Date: 2013-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 894496 - 2014-09-10](https://www.globalkeysolutions.net/api/records/fda_inspections/neuropace-inc/d0fee0d2-7c67-410a-8fd2-0bd0c9b14166/)
- [FDA Inspection 894496 - 2014-09-10](https://www.globalkeysolutions.net/api/records/fda_inspections/neuropace-inc/ec072779-c030-473f-8d55-bd747f30d89c/)
- [FDA Inspection 894496 - 2014-09-10](https://www.globalkeysolutions.net/api/records/fda_inspections/neuropace-inc/b3ea6ef7-6ef9-4d86-928d-f624d770dd86/)
- [FDA Inspection 823160 - 2013-03-05](https://www.globalkeysolutions.net/api/records/fda_inspections/neuropace-inc/2dfd68c1-1fb3-4852-8b54-f787b314b438/)
- [FDA Inspection 823160 - 2013-03-05](https://www.globalkeysolutions.net/api/records/fda_inspections/neuropace-inc/45b66d32-8ae2-4b65-8524-5cbf5611c331/)

Company: https://www.globalkeysolutions.net/companies/neuropace-inc/d137fe94-6710-4f75-b428-1fab81c1f601

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