FDA Inspection
Bausch & Lomb Surgical, Inc.Bausch & Lomb Surgical, Inc. – FDA Inspection, Nov 23, 2009
Record Details
This FDA Inspection record concerns Bausch & Lomb Surgical, Inc., with an inspection on November 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bausch & Lomb Surgical, Inc.
- Inspection Date
- November 23, 2009
- Product Type
- Devices
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ID · e5d1d726-3c77-4ee6-a8a7-8a4e3df8abe3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 629659
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 820.198(a)General
- 21 CFR 820.80(d)(1)DMR required activities {see also 820.181}
- 21 CFR 820.180Availability
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Other FDA inspections of Bausch & Lomb Surgical, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| June 28, 2024 | Not classified | Florida District Office | |
| November 3, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 5, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 30, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 18, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Bausch & Lomb Surgical, Inc.
- FDA Inspection 1248950 - 2024-06-28
- FDA Inspection 1030850 - 2017-11-03
- FDA Inspection 1008783 - 2017-04-05
- FDA Inspection 950005 - 2015-11-30
- FDA Inspection 926666 - 2015-05-18
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