FDA Inspection
Lymol Medical CorporationLymol Medical Corporation – FDA Inspection, Jul 9, 2009
Record Details
This FDA Inspection record concerns Lymol Medical Corporation, with an inspection on July 9, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Lymol Medical Corporation
- Inspection Date
- July 9, 2009
- Product Type
- Devices
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ID · 1d8a5bdf-2a74-4a64-ba5b-ac559afad610
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 596000
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.25(a)Training--operations, GMPs, written procedures
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Other FDA inspections of Lymol Medical Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| July 29, 2021 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 12, 2020 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 24, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 15, 2011 | VAI | Center for Drug Evaluation and Research | Postmarket Surv. and Epidemiology |
| September 14, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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