FDA Inspection
Peters SurgicalPeters Surgical – FDA Inspection, Dec 12, 2013
Record Details
This FDA Inspection record concerns Peters Surgical, with an inspection on December 12, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Peters Surgical
- Inspection Date
- December 12, 2013
- Product Type
- Devices
View Company Profile
ID · ba4253d4-8c73-4002-b5f3-6926133b51cd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 860539
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.22Quality audit - audit report review
- 21 CFR 820.50(a)(2)Supplier oversight
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.