FDA Inspection
Moor Instruments LtdMoor Instruments Ltd – FDA Inspection, Nov 7, 2019
Record Details
This FDA Inspection record concerns Moor Instruments Ltd, with an inspection on November 7, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Moor Instruments Ltd
- Inspection Date
- November 7, 2019
- Product Type
- Devices
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ID · 98039fa3-e5ea-4118-921d-ee1a21947288
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1109984
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
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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 |
| May 5, 2017 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| 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 1031124 - 2017-05-05
- FDA Inspection 894791 - 2014-08-21
- FDA Inspection 730020 - 2011-05-06
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