FDA Inspection
OtisMed, a Division of Stryker OrthopaedicsFDA Inspection 707834 - OtisMed, a Division of Stryker Orthopaedics - February 01, 2011
Record Details
This FDA Inspection record concerns OtisMed, a Division of Stryker Orthopaedics, with an inspection on February 1, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 1, 2011
- Product Type
- Devices
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ID · 25097fbc-34d2-4d8c-9eaa-120d33f67474