# LSI Solutions, Inc. – FDA Inspection, Oct 4, 2018

Source: https://www.keypedia.com/records/fda_inspections/lsi-solutions-inc/e54a6d0b-d485-4e78-9aad-f60545e769e4
Source feed: FDA_Inspections

> FDA inspection 1068513 of LSI Solutions, Inc., October 04, 2018. Classification: No Action Indicated (NAI). 2 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: 1068513
- Company Name: LSI Solutions, Inc.
- Inspection Date: 2018-10-04
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 855570 - 2013-11-01](https://www.keypedia.com/records/fda_inspections/lsi-solutions-inc/84053cdd-4019-4669-9788-f421b4bdd8e6)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-c-mendiola/387f053a-af5f-4da9-8042-031124b9467d)

Company: https://www.keypedia.com/companies/lsi-solutions-inc/e0d93f62-a133-496e-bc2c-eaf846393968

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