# Kronner Prototypes, Inc. dba Kronner Medical - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kronner-prototypes-inc-dba-kronner-medical/67fad6bb-e3e7-48c9-bd3c-cda19ecd864e

> Inspection records and compliance data for Kronner Prototypes, Inc. dba Kronner Medical in Roseburg, Oregon. Access full analysis and detailed observations.

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## Details

- Name: Kronner Prototypes, Inc. dba Kronner Medical
- FEI Number: 3018984
- City: Roseburg
- State: Oregon
- Country Name: United States
- Address Line 1: 1443 Upper Cleveland Rapids Rd
- Zip Code: 97471

## Related Documents

- [FDA Inspection 1009807 - Kronner Prototypes, Inc. dba Kronner Medical - 2017-04-12](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/76869c7b-b289-431e-996f-b687fd71b29c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2017
- [FDA Inspection 1009807 - Kronner Prototypes, Inc. dba Kronner Medical - 2017-04-12](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/1afc4ca1-0f60-40d5-8373-65b7a6acfd3f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2017
- [FDA Inspection 875081 - Kronner Prototypes, Inc. dba Kronner Medical - 2014-04-15](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/fefb49ed-36fc-40a3-b37d-1026b4028396) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 15, 2014
- [FDA Inspection 875081 - Kronner Prototypes, Inc. dba Kronner Medical - 2014-04-15](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/569c0bc0-4f19-4dd8-a59d-b5971d043212) — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2014
- [WARNING_LETTER - Kronner Prototypes, Inc. dba Kronner Medical - 2013-02-04](https://www.globalkeysolutions.net/records/warning_letter/kronner-prototypes-inc-dba-kronner-medical/2078b06e-83b2-4d70-bf1b-ac03bdcfc1e0) — source: FDA, date: February 4, 2013
- [FDA Inspection 816972 - Kronner Prototypes, Inc. dba Kronner Medical - 2013-02-04](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/8ca2b6f7-e820-46ea-be5f-e16f3976832f) — classification: Official Action Indicated (OAI), source: FDA, date: February 4, 2013
- [FDA Inspection 816972 - Kronner Prototypes, Inc. dba Kronner Medical - 2013-02-04](https://www.globalkeysolutions.net/records/fda_inspections/kronner-prototypes-inc-dba-kronner-medical/cbaed409-8399-41ee-bead-14d00ad42b9f) — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2013

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