FDA Inspection
Kammerer Medical Systems GmbH & Co. KGKammerer Medical Systems GmbH & Co. KG – FDA Inspection, Aug 30, 2018
Record Details
This FDA Inspection record concerns Kammerer Medical Systems GmbH & Co. KG, with an inspection on August 30, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- August 30, 2018
- Product Type
- Medical Devices & Rad Health
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ID · c904b1c0-2d79-4cb4-8fac-8912c172441d
Inspection Facts
- Inspection number
- 1063840
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.22Quality Audits - defined intervals
- 21 CFR 820.90(b)(2)Product rework documentation, DHR {see also 820.184}
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Other FDA inspections of Kammerer Medical Systems GmbH & Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 18, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 5, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kammerer Medical Systems GmbH & Co. KG
- FDA Inspection 1291146 - 2025-09-18
- FDA Inspection 915198 - 2015-02-05
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