# Fischer Medical Technologies, Inc. – FDA Inspection, Jun 5, 2009

Source: https://www.keypedia.com/records/fda_inspections/fischer-medical-technologies-inc/df588e99-d319-4451-8d7c-44203b70e75c
Source feed: FDA_Inspections

> FDA inspection 587950 of Fischer Medical Technologies, Inc., June 05, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 4

## Related Documents

- FDA Inspection 827080 - 2013-04-11

Company: https://www.keypedia.com/companies/fischer-medical-technologies-inc/2e5f3f36-165b-403f-9260-a4cb6992b43a

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