# FDA Inspection 1085112 - Rhein Manufacturing Inc - March 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/rhein-manufacturing-inc/67010857-1378-479c-acf3-28419c5a4de3
Source feed: FDA_Inspections

> FDA Inspection 1085112 for Rhein Manufacturing Inc on March 29, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085112
- Company Name: Rhein Manufacturing Inc
- Inspection Date: 2019-03-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1085112 - 2019-03-29](https://www.keypedia.com/records/fda_inspections/rhein-manufacturing-inc/a7f5586d-79c8-4e86-aa89-d2ab55fb9e80)

Company: https://www.keypedia.com/companies/rhein-manufacturing-inc/8d56aa2c-7eb1-4da2-85c0-28f3788bb1a8

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