# CAPTEK, Inc. – FDA Inspection, Sep 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/captek-inc/f65c1aa4-280c-439e-bd3e-54014dc18708
Source feed: FDA_Inspections

> FDA inspection 614651 of CAPTEK, Inc., September 25, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 614651
- Company Name: CAPTEK, Inc.
- Inspection Date: 2009-09-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

Company: https://www.keypedia.com/companies/captek-inc/9a8222e1-92ac-45b4-a5b8-24b3994cfc0e

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