FDA Inspection
Microstim Technology, Inc.Microstim Technology, Inc. – FDA Inspection, Jul 16, 2012
Record Details
This FDA Inspection record concerns Microstim Technology, Inc., with an inspection on July 16, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Microstim Technology, Inc.
- Inspection Date
- July 16, 2012
- Product Type
- Devices
View Company Profile
ID · c4e057d0-6973-4eb2-8876-492d68265bee
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 791510
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(b)Review and evaluation for investigation
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Microstim Technology, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 18, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 3, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Microstim Technology, Inc.
- FDA Inspection 997044 - 2016-11-18
- FDA Inspection 559883 - 2009-02-03
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