FDA Inspection
Ellis Ophthalmic Technologies, Inc.Ellis Ophthalmic Technologies, Inc. – FDA Inspection, Jan 8, 2013
Record Details
This FDA Inspection record concerns Ellis Ophthalmic Technologies, Inc., with an inspection on January 8, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 8, 2013
- Product Type
- Devices
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ID · 9ac8219f-aed3-4487-bae1-c6a8333fbbdd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 813406
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
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Other FDA inspections of Ellis Ophthalmic Technologies, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 4, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 25, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 18, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 26, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 11, 2008 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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