FDA Inspection
Bausch & Lomb IncBausch & Lomb Inc – FDA Inspection, Jun 10, 2016
Record Details
This FDA Inspection record concerns Bausch & Lomb Inc, with an inspection on June 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bausch & Lomb Inc
- Inspection Date
- June 10, 2016
- Product Type
- Devices
View Company Profile
ID · e6b707f0-594e-4de6-88ca-206f4902697f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 978030
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Bausch & Lomb Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 8, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 15, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 1, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 17, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bausch & Lomb Inc
- FDA Inspection 1107226 - 2019-10-08
- FDA Inspection 826558 - 2013-03-15
- FDA Inspection 784537 - 2012-06-01
- FDA Inspection 782300 - 2012-05-17
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