FDA Inspection
KDL Precision MoldingKDL Precision Molding – FDA Inspection, Jul 11, 2013
Record Details
This FDA Inspection record concerns KDL Precision Molding, with an inspection on July 11, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- KDL Precision Molding
- Inspection Date
- July 11, 2013
- Product Type
- Devices
View Company Profile
ID · adbb8961-eacd-4f28-bc82-c6711396edcd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 839847
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of KDL Precision Molding
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 7, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 1, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for KDL Precision Molding
- FDA Inspection 1079325 - 2019-02-07
- FDA Inspection 898384 - 2014-10-01
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