# Osteotec Limited – FDA Inspection, Sep 4, 2018

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

> FDA inspection 1064322 of Osteotec Limited, September 04, 2018. Classification: Official Action Indicated (OAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

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

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