FDA Inspection
ERCHINGERERCHINGER – FDA Inspection, Mar 5, 2015
Record Details
This FDA Inspection record concerns ERCHINGER, with an inspection on March 5, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- ERCHINGER
- Inspection Date
- March 5, 2015
- Product Type
- Devices
View Company Profile
ID · 4963428f-0682-4fac-9c4e-f827897e753f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 929018
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of ERCHINGER
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 4, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 29, 2018 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
Other documents for ERCHINGER
- FDA Inspection 1246506 - 2024-06-04
- FDA Inspection 1074967 - 2018-11-29
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