FDA Inspection
Lambda SpALambda SpA – FDA Inspection, Jul 27, 2017
Record Details
This FDA Inspection record concerns Lambda SpA, with an inspection on July 27, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Person
- Wendy R. Blame (Issuing Officer)
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ID · 3f68ba42-ca39-4462-8d95-026857230ca4
Inspection Facts
- Inspection number
- 1020377
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 1040.10(h)(2)(i)Reproduction of affixed information
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Lambda SpA
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 28, 2026 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
| October 19, 2023 | Not classified | Office of Inspections and Investigations | |
| May 17, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Lambda SpA
- FDA Inspection 1319174 - 2026-05-28
- FDA Inspection 1221088 - 2023-10-19
- FDA Inspection 832267 - 2013-05-17
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