# FDA Inspection 891110 - Pontis Orthopaedics, LLC - August 22, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/pontis-orthopaedics-llc/af27d35c-5636-443b-b91b-7acde138f0dd
Source feed: FDA_Inspections

> FDA Inspection 891110 for Pontis Orthopaedics, LLC on August 22, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891110
- Company Name: Pontis Orthopaedics, LLC
- Inspection Date: 2014-08-22
- 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 1058009 - 2018-07-05](https://www.globalkeysolutions.net/records/fda_inspections/pontis-orthopaedics-llc/9bc8a323-c944-4449-bf02-8be65cf4493e)
- [FDA Inspection 1058009 - 2018-07-05](https://www.globalkeysolutions.net/records/fda_inspections/pontis-orthopaedics-llc/a3074447-901b-443e-ba2e-9a2dae945c60)
- [FDA Inspection 891110 - 2014-08-22](https://www.globalkeysolutions.net/records/fda_inspections/pontis-orthopaedics-llc/66f42f47-21f2-4b71-bfd3-6d8f73799e02)

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

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