FDA Inspection
Perryman CompanyFDA Inspection 1106963 - Perryman Company - October 10, 2019
Record Details
This FDA Inspection record concerns Perryman Company, with an inspection on October 10, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Perryman Company
- Inspection Date
- October 10, 2019
- Product Type
- Devices
View Company Profile
ID · 0821bfd0-f144-4973-ad29-348a807f4c54
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1106963
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Perryman Company
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 10, 2026 | VAI | Philadelphia District Office | Compliance: Medical Devices |
| February 9, 2017 | NAI | 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 1005622 - 2017-02-09
- FDA Inspection 941493 - 2015-09-10
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