FDA Inspection
Axelgard Mfg Co LtdAxelgard Mfg Co Ltd – FDA Inspection, Jul 2, 2009
Record Details
This FDA Inspection record concerns Axelgard Mfg Co Ltd, with an inspection on July 2, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Axelgard Mfg Co Ltd
- Inspection Date
- July 2, 2009
- Product Type
- Devices
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ID · 84952e55-12cd-4682-a0f3-b10ec6b8e2e2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 595837
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.75(a)Documentation
- 21 CFR 820.250(b)Sampling plans
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Other FDA inspections of Axelgard Mfg Co Ltd
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 28, 2019 | Not classified | Los Angeles District Office |
Other documents for Axelgard Mfg Co Ltd
- FDA Inspection 1121812 - 2019-08-28
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