# FDA Inspection 1064322 - Osteotec Limited - September 04, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/osteotec-limited/ff62d752-b80f-440d-af10-4b399b17c146/
Source feed: FDA_Inspections

> FDA Inspection 1064322 for Osteotec Limited on September 04, 2018. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064322
- Company Name: Osteotec Limited
- Inspection Date: 2018-09-04
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1064322 - 2018-09-04](https://www.globalkeysolutions.net/api/records/fda_inspections/osteotec-limited/c417c1aa-1fd3-4e35-9aec-db4c40769545/)

Company: https://www.globalkeysolutions.net/companies/osteotec-limited/9522ca5b-7846-4d44-b2c6-c7a144f071bc

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