# Pontis Orthopaedics, LLC – FDA Inspection, Jul 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/pontis-orthopaedics-llc/a3074447-901b-443e-ba2e-9a2dae945c60
Source feed: FDA_Inspections

> FDA inspection 1058009 of Pontis Orthopaedics, LLC, July 05, 2018. Classification: No Action Indicated (NAI). 8 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: 1058009
- Company Name: Pontis Orthopaedics, LLC
- Inspection Date: 2018-07-05
- 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: 8

## Related Documents

- FDA Inspection 891110 - 2014-08-22

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/pontis-orthopaedics-llc/5991f036-2715-4626-a7da-503817f9a8af

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