FDA Inspection 1168317 — Spok, Inc.

Spok, Inc. — FEI 3014158829

The FDA completed an inspection of Spok, Inc. on April 29, 2022 in Alexandria, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 29, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Alexandria, VA (United States)

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
237121 CFR 820.30(a)Design control - no procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
317321 CFR 820.198(d)Evaluation, timeliness, identification
366521 CFR 820.20(b)(3)Management representative
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures