FDA Inspection
MDF Instruments Direct, Inc.MDF Instruments Direct, Inc. – FDA Inspection, May 3, 2012
Record Details
This FDA Inspection record concerns MDF Instruments Direct, Inc., with an inspection on May 3, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- MDF Instruments Direct, Inc.
- Inspection Date
- May 3, 2012
- Product Type
- Devices
View Company Profile
ID · b37b88cf-32fa-43d3-9f1c-31cc1df4fdfd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 780633
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.