# KDL Precision Molding – FDA Inspection, Jul 11, 2013

Source: https://www.keypedia.com/records/fda_inspections/kdl-precision-molding/adbb8961-eacd-4f28-bc82-c6711396edcd
Source feed: FDA_Inspections

> FDA inspection 839847 of KDL Precision Molding, July 11, 2013. Classification: Voluntary Action Indicated (VAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839847
- Company Name: KDL Precision Molding
- Inspection Date: 2013-07-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1079325 - 2019-02-07](https://www.keypedia.com/records/fda_inspections/kdl-precision-molding/258462f2-5fb8-4071-bfb2-d92955c5fe06)
- FDA Inspection 898384 - 2014-10-01

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

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