FDA Inspection
Cretex Medical -- Component and Device Technologies IncCretex Medical -- Component and Device Technologies Inc – FDA Inspection, Dec 19, 2017
Record Details
This FDA Inspection record concerns Cretex Medical -- Component and Device Technologies Inc, with an inspection on December 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 19, 2017
- Product Type
- Devices
- Person
- Seema S. Singh (Issuing Officer)
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ID · 5ea1da54-901b-45b6-91ff-b88db2ae39a8
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1036884
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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