# FDA Inspection 950318 - Zimmer Manufacturing B.V. - November 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/zimmer-manufacturing-bv/185da039-c087-4814-ba16-9f18afa8c1a9
Source feed: FDA_Inspections

> FDA Inspection 950318 for Zimmer Manufacturing B.V. on November 17, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 950318
- Company Name: Zimmer Manufacturing B.V.
- Inspection Date: 2015-11-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/zimmer-manufacturing-bv/06e36c6f-d5fb-4d03-a06c-9c6826faebc4

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