FDA Inspection
Perryman CompanyFDA Inspection 1005622 - Perryman Company - February 09, 2017
Record Details
This FDA Inspection record concerns Perryman Company, with an inspection on February 9, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perryman Company
- Inspection Date
- February 9, 2017
- Product Type
- Devices
View Company Profile
ID · dbf751bb-2ca9-4ce5-92b2-e08a36c4f188
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1005622
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Perryman Company
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 10, 2026 | VAI | Philadelphia District Office | Compliance: Medical Devices |
| October 10, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 10, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Perryman Company
- FDA Inspection 1307166 - 2026-03-10
- FDA Inspection 1106963 - 2019-10-10
- FDA Inspection 941493 - 2015-09-10
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