# Rhein Manufacturing Inc – FDA Inspection, Mar 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/rhein-manufacturing-inc/a7f5586d-79c8-4e86-aa89-d2ab55fb9e80
Source feed: FDA_Inspections

> FDA inspection 1085112 of Rhein Manufacturing Inc, March 29, 2019. Classification: No Action Indicated (NAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085112
- Company Name: Rhein Manufacturing Inc
- Inspection Date: 2019-03-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)

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