FDA Inspection
Trident Medical Products, IncTrident Medical Products, Inc – FDA Inspection, Feb 23, 2018
Record Details
This FDA Inspection record concerns Trident Medical Products, Inc, with an inspection on February 23, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · ace87918-5f2b-48e8-a790-f590ce7ad04a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1042236
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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