FDA Inspection
Acro Biotech Inc.Acro Biotech Inc. – FDA Inspection, May 1, 2018
Record Details
This FDA Inspection record concerns Acro Biotech Inc., with an inspection on May 1, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · cff77bf3-b41f-45a9-9283-85a0a321bc8f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1050458
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 803.17(a)(3)Lack of System for Timely Submission of Reports
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Acro Biotech Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 3, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Acro Biotech Inc.
- FDA Inspection 850016 - 2013-09-03
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