# Lenstec, Inc. – FDA Inspection, Nov 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/lenstec-inc/c4418754-4dcb-4145-8ddc-c62f97eda9a7
Source feed: FDA_Inspections

> FDA inspection 1030941 of Lenstec, Inc., November 01, 2017. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 803. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030941
- Company Name: Lenstec, Inc.
- Inspection Date: 2017-11-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 841056 - 2013-07-18](https://www.keypedia.com/records/fda_inspections/lenstec-inc/aff10c51-a40d-4d98-aeec-01d9f057aa98)
- FDA Inspection 761829 - 2012-01-24

## Related Officers

- [Joshua J. Silvestri](https://www.keypedia.com/people/joshua-j-silvestri/433e29b3-ce5f-44d2-9984-7a6cb61e1824)

Company: https://www.keypedia.com/companies/lenstec-inc/6890da6d-aeb3-4d21-8931-f7695e37342d

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