# FDA Inspection 1069151 - Jk Products Gmbh - September 21, 2018

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

> FDA Inspection 1069151 for Jk Products Gmbh on September 21, 2018. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1069151 - 2018-09-21](https://www.globalkeysolutions.net/records/fda_inspections/jk-products-gmbh/be4696cf-79d8-4419-8d32-e62edf17da67)
- [FDA Inspection 1069151 - 2018-09-21](https://www.globalkeysolutions.net/records/fda_inspections/jk-products-gmbh/d3333514-c875-4cd3-9fa3-e7a926f20fcc)
- [FDA Inspection 986132 - 2016-09-09](https://www.globalkeysolutions.net/records/fda_inspections/jk-products-gmbh/43687064-1fbc-481a-ac43-cb83f8cfd395)
- [FDA Inspection 986132 - 2016-09-09](https://www.globalkeysolutions.net/records/fda_inspections/jk-products-gmbh/378a1dae-fe4e-4951-8742-33dc1b7c2a62)

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

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