FDA Inspection
Cargille-Sacher Laboratories Inc.Cargille-Sacher Laboratories Inc. – FDA Inspection, Jun 8, 2012
Record Details
This FDA Inspection record concerns Cargille-Sacher Laboratories Inc., with an inspection on June 8, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 8, 2012
- Product Type
- Devices
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ID · 4b0ebd92-1017-46da-bddc-2c07ea677dd9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 786483
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
5- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.70(g)Equipment design and installation
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.184DHR content
- 21 CFR 820.50(b)Supplier notification of changes
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Other FDA inspections of Cargille-Sacher Laboratories Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2009 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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