# Nanovis LLC – FDA Inspection, Jul 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/nanovis-llc/f1e966c4-b3ae-4b13-bc7a-137e0a6be586
Source feed: FDA_Inspections

> FDA inspection 1059225 of Nanovis LLC, July 18, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059225
- Company Name: Nanovis LLC
- Inspection Date: 2018-07-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1308110 - 2026-03-19](https://www.keypedia.com/records/fda_inspections/nanovis-llc/f1cbd637-3cfb-4ee9-a75e-30b6016d2a46)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-j-gasparovich/478888db-d4b3-481a-89f5-ee234a160f07)

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

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