FDA Inspection
Lenstec, Inc.Lenstec, Inc. – FDA Inspection, Jul 18, 2013
Record Details
This FDA Inspection record concerns Lenstec, Inc., with an inspection on July 18, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lenstec, Inc.
- Inspection Date
- July 18, 2013
- Product Type
- Devices
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ID · aff10c51-a40d-4d98-aeec-01d9f057aa98
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 841056
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 820.198(d)Evaluation, timeliness, identification
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Lenstec, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 1, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 24, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Lenstec, Inc.
- FDA Inspection 1030941 - 2017-11-01
- FDA Inspection 761829 - 2012-01-24
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