FDA Inspection
Ackermann Usa IncAckermann Usa Inc – FDA Inspection, Aug 4, 2023
Record Details
This FDA Inspection record concerns Ackermann Usa Inc, with an inspection on August 4, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e45576bb-436c-4fe7-9f5f-488fe2d0302b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1211449
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
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