# Arbor Vita Corporation – FDA Inspection, Mar 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/arbor-vita-corporation/8dff8efd-f7f2-4c53-bd96-8b9423295622
Source feed: FDA_Inspections

> FDA inspection 822925 of Arbor Vita Corporation, March 18, 2013. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 822925
- Company Name: Arbor Vita Corporation
- Inspection Date: 2013-03-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1020816 - 2017-07-18
- [FDA Inspection 711127 - 2011-01-20](https://www.keypedia.com/records/fda_inspections/arbor-vita-corporation/c6c196ff-4a72-4564-9e9a-ddba82aa90a8)

Company: https://www.keypedia.com/companies/arbor-vita-corporation/40d99902-0027-41b8-87bb-c07038511338

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