# FDA Inspection 608672 - Glycadia, Inc dba Exocell - August 07, 2009

Source: https://www.keypedia.com/records/fda_inspections/glycadia-inc-dba-exocell/4377484a-cdc5-4e5c-957e-e77ee0982fbc
Source feed: FDA_Inspections

> FDA Inspection 608672 for Glycadia, Inc dba Exocell on August 07, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 608672
- Company Name: Glycadia, Inc dba Exocell
- Inspection Date: 2009-08-07
- 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/glycadia-inc-dba-exocell/235ca52b-b72e-47dc-add4-4eb0c4a5df64

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