# FDA Inspection 1079325 - KDL Precision Molding - February 07, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kdl-precision-molding/258462f2-5fb8-4071-bfb2-d92955c5fe06
Source feed: FDA_Inspections

> FDA Inspection 1079325 for KDL Precision Molding on February 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079325
- Company Name: KDL Precision Molding
- Inspection Date: 2019-02-07
- 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 1079325 - 2019-02-07](https://www.globalkeysolutions.net/records/fda_inspections/kdl-precision-molding/17fe844f-8d5e-447f-9f03-591616c3cd48)
- [FDA Inspection 898384 - 2014-10-01](https://www.globalkeysolutions.net/records/fda_inspections/kdl-precision-molding/6b85f096-7bbf-4263-b356-4ab1ef72f80e)
- [FDA Inspection 898384 - 2014-10-01](https://www.globalkeysolutions.net/records/fda_inspections/kdl-precision-molding/7f161bc2-738a-48f7-9923-0035c62d0d4f)
- [FDA Inspection 839847 - 2013-07-11](https://www.globalkeysolutions.net/records/fda_inspections/kdl-precision-molding/adbb8961-eacd-4f28-bc82-c6711396edcd)

Company: https://www.globalkeysolutions.net/companies/kdl-precision-molding/0c8495fe-9363-4065-8737-0bda13b09dae

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