FDA Inspection
Richter Rubber Technology Sdn BdhRichter Rubber Technology Sdn Bdh – FDA Inspection, Jun 2, 2016
Record Details
This FDA Inspection record concerns Richter Rubber Technology Sdn Bdh, with an inspection on June 2, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- June 2, 2016
- Product Type
- Devices
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ID · 01204912-0354-474c-9cb0-9e30763bf0b7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 979210
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.75(b)(2)Documentation of validated process performance
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Other FDA inspections of Richter Rubber Technology Sdn Bdh
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 20, 2025 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Richter Rubber Technology Sdn Bdh
- FDA Inspection 1265044 - 2025-02-20
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