FDA Inspection
Moor Instruments LtdMoor Instruments Ltd – FDA Inspection, May 5, 2017
Record Details
This FDA Inspection record concerns Moor Instruments Ltd, with an inspection on May 5, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 83177dfe-88a9-41af-9465-55368c281cf9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031124
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(b)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Moor Instruments Ltd
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 27, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 7, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 21, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 6, 2011 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Moor Instruments Ltd
- FDA Inspection 1191843 - 2022-10-27
- FDA Inspection 1109984 - 2019-11-07
- FDA Inspection 894791 - 2014-08-21
- FDA Inspection 730020 - 2011-05-06
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.