# FDA Inspection 698666 - K. W. Griffen Company DBA Biomed Packaging Systems - November 18, 2010

Source: https://www.keypedia.com/records/fda_inspections/k-w-griffen-company-dba-biomed-packaging-systems/a4957ac5-d51c-45cf-bdb2-83242fbbac3a
Source feed: FDA_Inspections

> FDA Inspection 698666 for K. W. Griffen Company DBA Biomed Packaging Systems on November 18, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 698666
- Company Name: K. W. Griffen Company DBA Biomed Packaging Systems
- Inspection Date: 2010-11-18
- Classification: No Action Indicated (NAI)
- 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/k-w-griffen-company-dba-biomed-packaging-systems/4f4e6ca6-e91b-44e7-a5d1-52537169f3a4

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