FDA Inspection
E-Teng Technology, Inc.E-Teng Technology, Inc. – FDA Inspection, Jul 14, 2016
Record Details
This FDA Inspection record concerns E-Teng Technology, Inc., with an inspection on July 14, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- E-Teng Technology, Inc.
- Inspection Date
- July 14, 2016
- Product Type
- Devices
View Company Profile
ID · 130248c6-da45-4909-b1c9-3f0e0bd3c383
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 987864
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.198(a)Complaints
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.90(a)Nonconforming product control
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Other FDA inspections of E-Teng Technology, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 15, 2024 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for E-Teng Technology, Inc.
- FDA Inspection 1242306 - 2024-05-15
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