FDA Inspection
Bausch & Lomb IncorporatedBausch & Lomb Incorporated – FDA Inspection, Feb 15, 2017
Record Details
This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on February 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 805afebf-54f2-435f-afe6-2044741ba093
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1001173
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(e)Records of complaint investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Bausch & Lomb Incorporated
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 9, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 9, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bausch & Lomb Incorporated
- FDA Inspection 909049 - 2014-12-09
- FDA Inspection 667094 - 2010-06-09
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.