FDA Inspection
Daily Medical Products, Inc.Daily Medical Products, Inc. – FDA Inspection, May 5, 2011
Record Details
This FDA Inspection record concerns Daily Medical Products, Inc., with an inspection on May 5, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Daily Medical Products, Inc.
- Inspection Date
- May 5, 2011
- Product Type
- Devices
View Company Profile
ID · cfa2a5a7-3871-4429-adf8-8edf05b5da90
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 724943
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.30(c)Design input - documentation
- 21 CFR 820.20(a)Management ensuring quality policy is understood
- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.50(b)Approval, inadequate purchasing data
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Daily Medical Products, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 21, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 6, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 29, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Daily Medical Products, Inc.
- FDA Inspection 1201082 - 2023-03-21
- FDA Inspection 1016104 - 2017-04-06
- FDA Inspection 853083 - 2013-10-29
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