FDA Inspection
Bausch & Lomb IncorporatedBausch & Lomb Incorporated – FDA Inspection, Jul 31, 2013
Record Details
This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on July 31, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Bausch & Lomb Incorporated
- Inspection Date
- July 31, 2013
- Product Type
- Devices
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ID · 2241014a-110c-45a1-9077-01bddc5ea0fc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 843014
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.75(a)Documentation
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Other FDA inspections of Bausch & Lomb Incorporated
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 9, 2018 | Not classified | New England District Office | |
| April 18, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Bausch & Lomb Incorporated
- FDA Inspection 1157054 - 2018-08-09
- FDA Inspection 720310 - 2011-04-18
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