# Amann Girrbach North America, L.P. – FDA Inspection, Aug 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/amann-girrbach-north-america-lp/fc66fff3-4929-451e-908c-1d1f4d944e71
Source feed: FDA_Inspections

> FDA inspection 1063743 of Amann Girrbach North America, L.P., August 29, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063743
- Company Name: Amann Girrbach North America, L.P.
- Inspection Date: 2018-08-29
- 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

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

Company: https://www.keypedia.com/companies/amann-girrbach-north-america-lp/84867189-9d0a-498e-ab59-618c43265eca

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