FDA Inspection
Unifirst-First Aid CorporationUnifirst-First Aid Corporation – FDA Inspection, Jul 13, 2015
Record Details
This FDA Inspection record concerns Unifirst-First Aid Corporation, with an inspection on July 13, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 13, 2015
- Product Type
- Devices
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ID · db622a08-e6c9-45dd-83a3-2363572d34e7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 934480
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
7- 21 CFR 211.150(b)Recall facilitation
- 21 CFR 211.137(d)Expiration date location on labeling
- 21 CFR 820.25(b)Training records
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.70(d)Implementing Personnel Procedures, Health, Cleanliness.
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Unifirst-First Aid Corporation
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 24, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 7, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Unifirst-First Aid Corporation
- FDA Inspection 1057223 - 2018-05-24
- FDA Inspection 679037 - 2010-09-07
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