# FDA Inspection 587950 - Fischer Medical Technologies, Inc. - June 05, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/fischer-medical-technologies-inc/773840ee-ef41-4c23-8094-8353f073db2d
Source feed: FDA_Inspections

> FDA Inspection 587950 for Fischer Medical Technologies, Inc. on June 05, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 587950
- Company Name: Fischer Medical Technologies, Inc.
- Inspection Date: 2009-06-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 827080 - 2013-04-11](https://www.globalkeysolutions.net/records/fda_inspections/fischer-medical-technologies-inc/9f73de1d-bb32-4d88-82a1-847b46cce372)
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Company: https://www.globalkeysolutions.net/companies/fischer-medical-technologies-inc/2e5f3f36-165b-403f-9260-a4cb6992b43a

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