# Baitella AG – FDA Inspection, Feb 2, 2012

Source: https://www.keypedia.com/records/fda_inspections/baitella-ag/a8df721e-9ab2-4b1f-9108-211e4bb6c681
Source feed: FDA_Inspections

> FDA inspection 770268 of Baitella AG, February 02, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 770268
- Company Name: Baitella AG
- Inspection Date: 2012-02-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1272814 - 2025-05-15
- FDA Inspection 972333 - 2016-05-18

Company: https://www.keypedia.com/companies/baitella-ag/55a06e9f-7cfd-4cf2-a3dd-94ff800ed12b

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