# Jk Products Gmbh – FDA Inspection, Sep 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/jk-products-gmbh/f0636f3d-f56b-4bff-98f7-c5260bd612ca
Source feed: FDA_Inspections

> FDA inspection 1069151 of Jk Products Gmbh, September 21, 2018. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069151
- Company Name: Jk Products Gmbh
- Inspection Date: 2018-09-21
- 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 Documents

- FDA Inspection 986132 - 2016-09-09

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maida-henesian/cd28e878-000c-4af8-8dbd-4863057758bb)

Company: https://www.keypedia.com/companies/jk-products-gmbh/64c9c29a-d7bd-4e44-88e6-36e65b157f18

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