# Straumann Manufacturing, Inc – FDA Inspection, Aug 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/straumann-manufacturing-inc/4a51c5d9-738c-410c-9b8f-18182a09da13
Source feed: FDA_Inspections

> FDA inspection 1064636 of Straumann Manufacturing, Inc, August 30, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064636
- Company Name: Straumann Manufacturing, Inc
- Inspection Date: 2018-08-30
- 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: 2

## Related Officers

- [Investigator](https://www.keypedia.com/people/akbar-j-zaidi/9cd9ac91-2d4b-4f6f-a975-865342075924)

Company: https://www.keypedia.com/companies/straumann-manufacturing-inc/817ab580-95f5-4b36-b563-c67077f13cb4

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