FDA Inspection
Life Recovery Systems HD, LLCLife Recovery Systems HD, LLC – FDA Inspection, Oct 21, 2019
Record Details
This FDA Inspection record concerns Life Recovery Systems HD, LLC, with an inspection on October 21, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 21, 2019
- Product Type
- Devices
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ID · e35a9ba7-a79d-4209-83d6-128745d14d51
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1106961
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Life Recovery Systems HD, LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 5, 2026 | Not classified | New Jersey District Office | Compliance: Medical Devices |
| September 11, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 14, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 14, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 4, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Life Recovery Systems HD, LLC
- FDA Inspection 1302344 - 2026-02-05
- FDA Inspection 1218858 - 2023-09-11
- FDA Inspection 969065 - 2016-03-14
- FDA Inspection 794489 - 2012-08-14
- FDA Inspection 761055 - 2012-01-04
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