FDA Inspection
Limerick IncLimerick Inc – FDA Inspection, Dec 7, 2012
Record Details
This FDA Inspection record concerns Limerick Inc, with an inspection on December 7, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Limerick Inc
- Inspection Date
- December 7, 2012
- Product Type
- Devices
View Company Profile
ID · 95684490-1438-4c7d-a300-a10925a7aac5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 810442
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Limerick Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 15, 2025 | NAI | Los Angeles District Office | Postmarket Assurance: Medical Devices |
| August 26, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 6, 2018 | Not classified | Los Angeles District Office | |
| February 11, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 25, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Limerick Inc
- FDA Inspection 1278581 - 2025-08-15
- FDA Inspection 1150394 - 2021-08-26
- FDA Inspection 1060071 - 2018-03-06
- FDA Inspection 914704 - 2015-02-11
- FDA Inspection 571611 - 2009-02-25
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