FDA Inspection
Tanses Technologies Inc.Tanses Technologies Inc. – FDA Inspection, May 26, 2017
Record Details
This FDA Inspection record concerns Tanses Technologies Inc., with an inspection on May 26, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Person
- Li Li (Issuing Officer)
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ID · f4d2fb12-98eb-458b-b899-34a599710160
Inspection Facts
- Inspection number
- 1017477
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 1010.2(c)Certification not based on adequate test/testing program
- 21 CFR 1040.20(d)(1)(iv)Recommended exposure schedule
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Tanses Technologies Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 5, 2019 | Not classified | Office of Inspections and Investigations |
Other documents for Tanses Technologies Inc.
- FDA Inspection 1141268 - 2019-09-05
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