FDA Inspection
Bausch & Lomb Ireland LimitedBausch & Lomb Ireland Limited – FDA Inspection, Nov 16, 2018
Record Details
This FDA Inspection record concerns Bausch & Lomb Ireland Limited, with an inspection on November 16, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- November 16, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 03a430d5-6b50-4518-a390-d8de360658a8
Inspection Facts
- Inspection number
- 1102223
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Bausch & Lomb Ireland Limited
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 1, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 15, 2017 | Not classified | Office of Inspections and Investigations | |
| February 17, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 9, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Bausch & Lomb Ireland Limited
- FDA Inspection 1179049 - 2022-07-01
- FDA Inspection 1042514 - 2017-09-15
- FDA Inspection 1008319 - 2017-02-17
- FDA Inspection 744844 - 2011-08-09
- FDA Inspection 739708 - 2011-07-21
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