# FDA Inspection 589018 - Turntine Ocular Prosthetics Inc - June 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/turntine-ocular-prosthetics-inc/83897e7f-9ed1-4bd1-9f41-1138007aa590
Source feed: FDA_Inspections

> FDA Inspection 589018 for Turntine Ocular Prosthetics Inc on June 10, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 589018
- Company Name: Turntine Ocular Prosthetics Inc
- Inspection Date: 2009-06-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 821734 - 2013-02-14](https://www.keypedia.com/records/fda_inspections/turntine-ocular-prosthetics-inc/1dc6484b-403c-4421-aae0-25a8b15bd6df)
- [FDA Inspection 821734 - 2013-02-14](https://www.keypedia.com/records/fda_inspections/turntine-ocular-prosthetics-inc/613f4ebb-2fa1-4fa8-b2b0-69cb47496ca9)

Company: https://www.keypedia.com/companies/turntine-ocular-prosthetics-inc/22f19d53-ac00-429f-bd0d-cbdc8ce8b7d0

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