# FDA Inspection 895402 - Cytophil, Inc. - September 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/cytophil-inc/4fed4761-14a2-4261-bab4-0ced3efb8b46
Source feed: FDA_Inspections

> FDA Inspection 895402 for Cytophil, Inc. on September 15, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 895402
- Company Name: Cytophil, Inc.
- Inspection Date: 2014-09-15
- 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/cytophil-inc/e476776c-5926-4d3e-97f0-b78bc379bc43

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