FDA Inspection
AAP Implantate AgAAP Implantate Ag – FDA Inspection, Mar 15, 2012
Record Details
This FDA Inspection record concerns AAP Implantate Ag, with an inspection on March 15, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- AAP Implantate Ag
- Inspection Date
- March 15, 2012
- Product Type
- Devices
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ID · ab41719c-f390-4ee5-a067-fc407ffcd1a4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 772646
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
- 21 CFR 820.250(b)Sampling plans
Full citation text and observation details available on the Dashboard.
Other FDA inspections of AAP Implantate Ag
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 11, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 4, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 7, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 17, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 12, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for AAP Implantate Ag
- FDA Inspection 1286384 - 2025-09-11
- FDA Inspection 1192265 - 2022-11-04
- FDA Inspection 1111642 - 2019-11-07
- FDA Inspection 1017003 - 2017-05-17
- FDA Inspection 917531 - 2015-02-12
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