# Straumann USA LLC – FDA Inspection, Jul 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/straumann-usa-llc/f57f061c-13d5-4966-9105-ff7700d6a182
Source feed: FDA_Inspections

> FDA inspection 1019048 of Straumann USA LLC, July 21, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803, 806, 820 and 1271. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019048
- Company Name: Straumann USA LLC
- Inspection Date: 2017-07-21
- 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: 6

## Related Documents

- FDA Inspection 1122746 - 2020-03-04
- FDA Inspection 903595 - 2014-11-13
- FDA Inspection 903433 - 2014-11-13

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/elizabeth-b-griffin/5567685a-c657-4710-afee-e7af8875b605)

Company: https://www.keypedia.com/companies/straumann-usa-llc/9a27e5b2-2d25-4a71-a1d2-0cfda8b41aa0

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