FDA Inspection
Bausch & Lomb IncorporatedBausch & Lomb Incorporated – FDA Inspection, Aug 18, 2017
Record Details
This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on August 18, 2017, issued by the New York District Office, covering medical devices & rad health.
- Company
- Bausch & Lomb Incorporated
- Inspection Date
- August 18, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- New York District Office
View Company Profile
ID · e7571e46-b1d2-43bc-8550-1b2233f7c9b7
Inspection Facts
- Inspection number
- 1042383
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Bausch & Lomb Incorporated
10| Date | Classification | Office | Project area |
|---|---|---|---|
| July 30, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 9, 2024 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| November 25, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 23, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 24, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Bausch & Lomb Incorporated
- FDA Inspection 1282260 - 2025-07-30
- FDA Inspection 1250019 - 2024-09-09
- FDA Inspection 1110911 - 2019-11-25
- FDA Inspection 1042701 - 2018-02-23
- FDA Inspection 1007875 - 2017-03-24
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