# FDA Inspection 1098911 - LUBRINOVATION, Inc. - August 07, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/lubrinovation-inc/dc98968e-e06d-4043-ba9b-5b80fc1a7570
Source feed: FDA_Inspections

> FDA Inspection 1098911 for LUBRINOVATION, Inc. on August 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098911
- Company Name: LUBRINOVATION, Inc.
- Inspection Date: 2019-08-07
- 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 1098911 - 2019-08-07](https://www.globalkeysolutions.net/records/fda_inspections/lubrinovation-inc/41750046-bc09-4d0c-8b7e-b4a3bbd14dc8)

Company: https://www.globalkeysolutions.net/companies/lubrinovation-inc/312fa5c6-a8d0-4dbe-a177-d237207c59a6

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