FDA Inspection
Kinetic Instruments, Inc.Kinetic Instruments, Inc. – FDA Inspection, Jan 6, 2016
Record Details
This FDA Inspection record concerns Kinetic Instruments, Inc., with an inspection on January 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kinetic Instruments, Inc.
- Inspection Date
- January 6, 2016
- Product Type
- Devices
View Company Profile
ID · c22f1f78-8f83-4356-86a3-779b563f6500
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 955255
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Kinetic Instruments, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kinetic Instruments, Inc.
- FDA Inspection 1100800 - 2019-08-14
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