# PFM Medical Titanium GmbH – FDA Inspection, Jul 9, 2009

Source: https://www.keypedia.com/records/fda_inspections/pfm-medical-titanium-gmbh/eecc30c1-3a20-4caf-b297-a188dcb5aab3
Source feed: FDA_Inspections

> FDA inspection 599820 of PFM Medical Titanium GmbH, 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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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