# FDA Inspection 599820 - PFM Medical Titanium GmbH - July 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/pfm-medical-titanium-gmbh/56adce74-518e-41d0-91e0-5c3b1f96c646
Source feed: FDA_Inspections

> FDA Inspection 599820 for PFM Medical Titanium GmbH on July 09, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 599820
- Company Name: PFM Medical Titanium GmbH
- Inspection Date: 2009-07-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 599820 - 2009-07-09](https://www.keypedia.com/records/fda_inspections/pfm-medical-titanium-gmbh/eecc30c1-3a20-4caf-b297-a188dcb5aab3)

Company: https://www.keypedia.com/companies/pfm-medical-titanium-gmbh/4bb91f5c-302c-4ff8-b68b-b95dd90eca65

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