FDA Inspection
Healthline Medical Products, Inc.Healthline Medical Products, Inc. – FDA Inspection, Jan 8, 2010
Record Details
This FDA Inspection record concerns Healthline Medical Products, Inc., with an inspection on January 8, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 8, 2010
- Product Type
- Devices
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ID · 77b4c153-41da-4c09-ae79-5b32cbb3db03
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 637368
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)General
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Healthline Medical Products, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 1, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 24, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 16, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 13, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Healthline Medical Products, Inc.
- FDA Inspection 1254996 - 2024-11-05
- FDA Inspection 1209742 - 2023-06-01
- FDA Inspection 1107841 - 2019-10-24
- FDA Inspection 1014941 - 2017-06-16
- FDA Inspection 822075 - 2013-03-13
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