FDA Inspection
Remote Technologies, Inc.Remote Technologies, Inc. – FDA Inspection, Sep 14, 2017
Record Details
This FDA Inspection record concerns Remote Technologies, Inc., with an inspection on September 14, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 1814c751-cb38-4327-9b5c-bfd54470544f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1025152
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.72(b)Calibration procedures - content
- 21 CFR 820.198(c)Investigation of device failures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Remote Technologies, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 8, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 13, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 21, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Remote Technologies, Inc.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.