# FDA Inspection 1059225 - Nanovis LLC - July 18, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/nanovis-llc/15070190-c6fb-4062-9742-2f31b954fb6f
Source feed: FDA_Inspections

> FDA Inspection 1059225 for Nanovis LLC on July 18, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1059225
- Company Name: Nanovis LLC
- Inspection Date: 2018-07-18
- 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 1308110 - 2026-03-19](https://www.globalkeysolutions.net/records/fda_inspections/nanovis-llc/275cb846-566e-45db-9084-0fd41e07c0bb)
- [FDA Inspection 1308110 - 2026-03-19](https://www.globalkeysolutions.net/records/fda_inspections/nanovis-llc/d9a13793-e75d-4650-a0b7-1e521214a0d7)
- [FDA Inspection 1059225 - 2018-07-18](https://www.globalkeysolutions.net/records/fda_inspections/nanovis-llc/f1e966c4-b3ae-4b13-bc7a-137e0a6be586)

Company: https://www.globalkeysolutions.net/companies/nanovis-llc/9b7f44c3-1740-4ccf-ac0e-742df8a5da75

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