FDA Inspection
Bausch & Lomb, Inc.Bausch & Lomb, Inc. – FDA Inspection, Nov 22, 2024
Record Details
This FDA Inspection record concerns Bausch & Lomb, Inc., with an inspection on November 22, 2024, issued by the Kansas City District Office, covering medical devices & rad health.
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ID · 099a5d4e-8305-49ef-ac18-4b988c8571ac
Inspection Facts
- Inspection number
- 1251448
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Medical Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
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Other FDA inspections of Bausch & Lomb, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 10, 2019 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| June 9, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 28, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 19, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Bausch & Lomb, Inc.
- FDA Inspection 1107243 - 2019-10-10
- FDA Inspection 973794 - 2016-06-09
- FDA Inspection 876296 - 2014-04-28
- FDA Inspection 766406 - 2012-01-19
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