FDA Inspection
Bausch & Lomb, IncorporatedBausch & Lomb, Incorporated – FDA Inspection, Jul 13, 2018
Record Details
This FDA Inspection record concerns Bausch & Lomb, Incorporated, with an inspection on July 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7d228ae0-876d-4816-9904-3d209ef90540
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1058969
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product control
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Other FDA inspections of Bausch & Lomb, Incorporated
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 4, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 28, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bausch & Lomb, Incorporated
- FDA Inspection 893517 - 2014-08-13
- FDA Inspection 847745 - 2013-09-04
- FDA Inspection 682741 - 2010-09-28
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